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Trial registered on ANZCTR
Registration number
ACTRN12611000569909
Ethics application status
Approved
Date submitted
2/06/2011
Date registered
3/06/2011
Date last updated
7/04/2014
Type of registration
Retrospectively registered
Titles & IDs
Public title
Oral Silodosin on Lower Urinary Tract Symptoms Due to Double-J stent: A Prospectively Randomized Study
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Scientific title
Oral silodosin on lower urinary tract symptoms due to double-J stent
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Secondary ID [1]
262296
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Nil
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Universal Trial Number (UTN)
U1111-1121-8585
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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:
urinary symptoms assosciated with indwelling double-J ureteral stents
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Condition category
Condition code
Renal and Urogenital
268133
268133
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0
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Other renal and urogenital disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
daily oral silodosin 4 mg for 2 weeks in improving symptoms and quality of life in patients with indwelling double-J ureteral stents using specific questionnaire
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Intervention code [1]
266688
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Treatment: Drugs
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Comparator / control treatment
daily oral lactose tablet for 2 weeks
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Control group
Placebo
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Outcomes
Primary outcome [1]
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ureteral stent symptom questionnaire (USSQ) evaluating the symptoms associated with double-J stents
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Assessment method [1]
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Timepoint [1]
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at 2nd week and 4th week
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Primary outcome [2]
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quality of life of International Prostate Symptom Scale (IPSS) evaluating the symptoms associated with double-J stents
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Assessment method [2]
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Timepoint [2]
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at 2nd week and 4th week
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Secondary outcome [1]
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Nil
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Assessment method [1]
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Timepoint [1]
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Nil
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Eligibility
Key inclusion criteria
patients, with insertion of a double-J ureteral stent after ureteroscopic stone removal, were enrolled into the study
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Minimum age
20
Years
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Maximum age
60
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
benign prostatic hyperplasia-related lower urinary symptoms(International Prostate Symptom Score greater greater than 7); a history of interstitial cystitis, chronic cystitis, chronic prostatitis, or stent insertion; and chronic medication with alpha-blockers or analgesics
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
numbered containers
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
random numbers table
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 4
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/11/2010
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Actual
1/11/2010
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Date of last participant enrolment
Anticipated
30/04/2012
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Actual
30/04/2012
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
45
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
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Taiwan, Province Of China
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State/province [1]
3610
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Funding & Sponsors
Funding source category [1]
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Self funded/Unfunded
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Name [1]
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Chung Jing Wang
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Address [1]
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60058 No 565 2nd Ta-Ya Rd, Chia-Yi city,Taiwan,ROC
St Martin De Porres Hospital
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Country [1]
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Taiwan, Province Of China
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Primary sponsor type
Individual
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Name
Chung Jing Wang
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Address
60058 No 565 2nd Ta-Ya Rd, Chia-Yi city,Taiwan,ROC
St Martin De Porres Hospital
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Country
Taiwan, Province Of China
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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]
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Country [1]
266250
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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IRB STM
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Ethics committee address [1]
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60058 No 565 2nd Rd Ta-Ya Chia-Yi city,Taiwan ROC St Martin De Porres Hospital
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Ethics committee country [1]
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Taiwan, Province Of China
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Date submitted for ethics approval [1]
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28/06/2010
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Approval date [1]
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21/07/2010
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Ethics approval number [1]
269171
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Summary
Brief summary
a randomized double-blinded controlled study to evaluate the effect of silodosin in improving symptoms and quality of life in patients with indwelling double-J ureteral stents using specific questionnaire
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Trial website
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Trial related presentations / publications
not yet
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Public notes
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Contacts
Principal investigator
Name
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A/Prof Chung Jing Wang
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Address
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60058 No 565 2nd Ta-Ya Rd, Chia-Yi city,Taiwan,ROC
St Martin De Porres Hospital
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Country
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Taiwan, Province Of China
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Phone
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886-5-2756000-1013
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Fax
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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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Chung Jing Wang
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Address
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60058 No 565 2nd Ta-Ya Rd, Chia-Yi city,Taiwan,ROC
St Martin De Porres Hospital
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Country
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Taiwan, Province Of China
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Phone
15937
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886-5-2756000-1013
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Fax
15937
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886-5-2788535
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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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Chung Jing Wang
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Address
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60058 No 565 2nd Ta-Ya Rd, Chia-Yi city,Taiwan,ROC
St Martin De Porres Hospital
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Country
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Taiwan, Province Of China
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Phone
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886-5-2756000-1013
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Fax
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886-5-2788535
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Email
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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
No additional documents have been identified.
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