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Trial registered on ANZCTR
Registration number
ACTRN12610000558022
Ethics application status
Approved
Date submitted
7/07/2010
Date registered
12/07/2010
Date last updated
17/02/2014
Type of registration
Prospectively registered
Titles & IDs
Public title
A prospective non-interventional study to evaluate the effect of Triptorelin Embonate (Diphereline (Trademark TM) 11.25mg) on lower urinary tract symptoms (LUTS) in Australian prostate cancer patients.
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Scientific title
A prospective non-interventional study to evaluate the effect of Triptorelin Embonate (Diphereline (TM) 11.25mg) on lower urinary tract symptoms (LUTS) in Australian prostate cancer patients.
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Secondary ID [1]
252037
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Ipsen Proprietary Limited
A-9B-52014-179
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Locally advanced or metastatic prostate cancer with Lower Urinary Tract Symptoms (LUTS)
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Condition category
Condition code
Cancer
257752
257752
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0
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Prostate
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Renal and Urogenital
257888
257888
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0
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Other renal and urogenital disorders
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Intervention/exposure
Study type
Observational
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
This is an observational study investigating the effect of Triptorelin Embonate (Diphereline (TM) 11.25mg) on lower urinary tract symptoms (LUTS) in Australian prostate cancer patients. The study participation duration for each patient will be 48 weeks. Each subject will receive 4 intramuscular injections of the Triptorelin Embonate (Diphereline (TM) 11.25mg) every 12 weeks at baseline, weeks 12, 24 and 36.
This study is collecting data about the subject’s normal treatment with Triptorelin Embonate (Diphereline (TM)) looking at the effect of this drug on lower urinary tract symptoms (LUTS) in Australian prostate cancer patients. The subject will continue to be treated for prostate cancer according to the best medical practice in Australia. The subject's medical care will not change in anyway as a result of the study and no additional tests or examinations are needed. The only difference will be that subject’s medical details will be recorded not only as it is routinely done in their clinic notes, but also anonymously in an electronic database.
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Intervention code [1]
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Not applicable
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Comparator / control treatment
No comparator
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Evaluation of the percentage of patients suffering from prostate cancer with moderate to severe LUTS (score International Prostate Symptom Score (IPSS) >7) with at-least 3 points reduction of IPSS score at the end of study week 48 (W48)
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Assessment method [1]
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Timepoint [1]
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48 weeks after baseline.
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Secondary outcome [1]
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Evaluation of percentage of patients suffering from prostate cancer with moderate to severe LUTS (score IPSS >7) with at-least 3 points reduction of IPSS score at week 24.
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Assessment method [1]
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Timepoint [1]
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24 weeks after baseline.
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Secondary outcome [2]
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Correlation between IPSS score changes and total Prostate Specific Antigen (PSA) changes after 24 weeks of treatment compared to baseline in patients with non-operable prostate cancer presenting moderate to severe LUTS (score IPSS > 7) at baseline.
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Assessment method [2]
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Timepoint [2]
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At baseline and at 24 weeks after baseline.
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Secondary outcome [3]
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Correlation between IPSS score changes and total PSA changes after 48 weeks of treatment compared to baseline in patients with prostate cancer presenting moderate to severe LUTS (score IPSS >7) at baseline
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Assessment method [3]
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Timepoint [3]
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At baseline and at 48 weeks after baseline.
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Secondary outcome [4]
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The correlation between IPSS score changes and Qmax (Maximum Urinary Flow Rate) as measured by flowmetry changes after 48 weeks of treatment compared to baseline in patients with prostate cancer presenting with moderate to severe LUTS (score IPSS >7) at baseline
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Assessment method [4]
264625
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Timepoint [4]
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At baseline and at 48 weeks after baseline.
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Eligibility
Key inclusion criteria
1.The patient is suffering from locally-advanced (at least Tumour 3 stage) or metastatic prostate cancer scheduled to receive Diphereline (TM) 11.25mg.
2.The patient is presenting with moderate to severe LUTS ((lower urinary tract symptoms) IPSS score >7).
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Males
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Can healthy volunteers participate?
No
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Key exclusion criteria
1.The patient has a risk of serious complication in the case of tumour flare (vertbral metastases threatening spinal cord compression or significant obstructive uropathy).
2.History of surgical castration.
3.History of urethral stricture.
4.Life expectancy of less than 12 months.
5.Has undergone surgery for the treatment of lower urinary tract symptoms(LUTS).
6.Therapy with a Luteinizing hormone-releasing hormone (LHRH) analogue in the last 6 months.
7. Has received alpha receptor blockers in the last two weeks prior to the start of the study.
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Active, not recruiting
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Date of first participant enrolment
Anticipated
15/10/2010
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Actual
8/03/2011
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Date of last participant enrolment
Anticipated
28/06/2013
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Actual
12/06/2013
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
70
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,SA,VIC
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Recruitment hospital [1]
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Sydney Adventist Hospital - Wahroonga
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Recruitment hospital [2]
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Repatriation Hospital - Daw Park
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Recruitment hospital [3]
2105
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Austin Health - Austin Hospital - Heidelberg
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Recruitment hospital [4]
2106
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The Alfred - Prahran
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Recruitment hospital [5]
2107
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Figtree Private Hospital - Figtree
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Recruitment hospital [6]
2108
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Epworth Richmond - Richmond
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Recruitment hospital [7]
2109
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Brisbane Private Hospital - Brisbane
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Recruitment hospital [8]
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Riverina Cancer Care Centre - Wagga Wagga
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Recruitment hospital [9]
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Mount Hospital - Perth
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Recruitment postcode(s) [1]
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2076 - Wahroonga
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Recruitment postcode(s) [2]
7796
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5041 - Daw Park
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Recruitment postcode(s) [3]
7797
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3084 - Heidelberg
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Recruitment postcode(s) [4]
7798
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3004 - Melbourne
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Recruitment postcode(s) [5]
7799
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2525 - Figtree
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Recruitment postcode(s) [6]
7800
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3121 - Richmond
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Recruitment postcode(s) [7]
7801
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4000 - Brisbane
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Recruitment postcode(s) [8]
7802
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2650 - Wagga Wagga
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Recruitment postcode(s) [9]
7803
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6000 - Perth
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Funding & Sponsors
Funding source category [1]
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Commercial sector/Industry
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Name [1]
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Ipsen Pty Ltd
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Address [1]
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Level 2, Building 4, Brandon Office Park,
540 Springvale Road,
Glen Waverley, VIC, 3150
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Country [1]
257160
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Australia
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Primary sponsor type
Commercial sector/Industry
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Name
Ipsen Pty Ltd
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Address
Level 2, Building 4, Brandon Office Park,
540 Springvale Road,
Glen Waverley, VIC, 3150
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
256416
0
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Country [1]
256416
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
259282
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Flinders Clinical Research Ethics Committee
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Ethics committee address [1]
259282
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Human Research and Ethics Department Room 2A221 Flinders Medical Centre Flinders Drive BEDFORD PARK SA 5042
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Ethics committee country [1]
259282
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Australia
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Date submitted for ethics approval [1]
259282
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19/07/2010
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Approval date [1]
259282
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22/10/2010
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Ethics approval number [1]
259282
0
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Ethics committee name [2]
290578
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Adventist HealthCare Ltd HREC
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Ethics committee address [2]
290578
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Adventist HealthCare Limited Australasian Research Institute Building 185 Fox Valley Road WAHROONGA NSW 2076
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Ethics committee country [2]
290578
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Australia
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Date submitted for ethics approval [2]
290578
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25/01/2011
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Approval date [2]
290578
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01/04/2011
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Ethics approval number [2]
290578
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EC00141
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Ethics committee name [3]
290579
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The Southern Adelaide Clinical Human Research Ethics Committee (SAC HREC)
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Ethics committee address [3]
290579
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The Flats G5 Flinders Drive c/- Flinders Medical Centre BEDFORD PARK SA 5042
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Ethics committee country [3]
290579
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Australia
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Date submitted for ethics approval [3]
290579
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01/07/2010
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Approval date [3]
290579
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22/10/2010
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Ethics approval number [3]
290579
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EC00188
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Ethics committee name [4]
290580
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Austin Health Human Research Ethics Committee
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Ethics committee address [4]
290580
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Office for Research Harold Stokes Building 145 Studley Rd HEIDELBERG VIC 3084
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Ethics committee country [4]
290580
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Australia
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Date submitted for ethics approval [4]
290580
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13/05/2011
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Approval date [4]
290580
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04/04/2012
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Ethics approval number [4]
290580
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EC00204
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Ethics committee name [5]
290581
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Alfred Hospital Ethics Committee
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Ethics committee address [5]
290581
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Alfred Hospital Commercial Road MELBOURNE VIC 3004
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Ethics committee country [5]
290581
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Australia
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Date submitted for ethics approval [5]
290581
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31/05/2012
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Approval date [5]
290581
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14/12/2012
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Ethics approval number [5]
290581
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EC00315
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Ethics committee name [6]
290582
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Joint University of Wollongong and Illawarra Shoalhaven Local Health District Health and Medical Human Research Ethics Committee
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Ethics committee address [6]
290582
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Ethics Unit Building 20, Level 1 (Research Services Office) University of Wollongong WOLLONGONG NSW 2522
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Ethics committee country [6]
290582
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Australia
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Date submitted for ethics approval [6]
290582
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28/02/2011
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Approval date [6]
290582
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11/07/2011
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Ethics approval number [6]
290582
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EC00150
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Ethics committee name [7]
290583
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Epworth HealthCare Human Research Ethics Committee
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Ethics committee address [7]
290583
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Epworth HealthCare 89 Bridge Road 5LP RICHMOND VIC 3121
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Ethics committee country [7]
290583
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Australia
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Date submitted for ethics approval [7]
290583
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15/09/2010
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Approval date [7]
290583
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08/10/2010
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Ethics approval number [7]
290583
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EC00217
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Ethics committee name [8]
290584
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Bellberry Human Research Ethics Committee A
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Ethics committee address [8]
290584
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129 Glen Osmond Road 81 Flinders Street Eastwood SA 5063
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Ethics committee country [8]
290584
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Australia
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Date submitted for ethics approval [8]
290584
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08/08/2011
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Approval date [8]
290584
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29/08/2011
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Ethics approval number [8]
290584
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EC00372
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Ethics committee name [9]
290585
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Mount Hospital Ethics Committee
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Ethics committee address [9]
290585
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Mount Hospital Ethics Committee 150 Mounts Bay Road PERTH WA 6000
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Ethics committee country [9]
290585
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Australia
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Date submitted for ethics approval [9]
290585
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01/11/2010
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Approval date [9]
290585
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06/04/2011
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Ethics approval number [9]
290585
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EC00387
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Summary
Brief summary
This study will collect information from routine clinical care with the intention of evaluating the effect of Diphereline on the symptoms that are present in many men with prostate cancer, such as difficulty in postponing urination, how often they have a weak urinary stream and/or the need to push or strain to begin urination. These symptoms are referred to as lower urinary tract symptoms (LUTS).
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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A/Prof Henry Woo
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Address
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San Clinic, Suite 406
185 Fox Valley Road
Wahroonga, NSW, 2076
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Country
31299
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Australia
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Phone
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+61 2 9473 8765
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Fax
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+61 2 9473 8969
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Email
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[email protected]
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Contact person for public queries
Name
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Jay Dharma
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Address
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Ipsen Pty Ltd.
Level 2, Building 4, Brandon Office Park,
540 Springvale Road,
Glen Waverley, VIC, 3150
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Country
14546
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Australia
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Phone
14546
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+ 61 3 8544 8100
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Fax
14546
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+ 61 3 9562 5152
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Email
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[email protected]
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Contact person for scientific queries
Name
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Monica de Abadal
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Address
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Ipsen Pty Ltd.
Level 2, Building 4, Brandon Office Park,
540 Springvale Road,
Glen Waverley, VIC, 3150
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Country
5474
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Australia
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Phone
5474
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+ 61 3 8544 8100
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Fax
5474
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+61 3 9562 5152
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Email
5474
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Effect of triptorelin on lower urinary tract symptoms in Australian prostate cancer patients.
2017
https://dx.doi.org/10.2147/RRU.S125791
N.B. These documents automatically identified may not have been verified by the study sponsor.
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