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Trial registered on ANZCTR
Registration number
ACTRN12616001166460
Ethics application status
Approved
Date submitted
15/08/2016
Date registered
26/08/2016
Date last updated
11/08/2017
Type of registration
Retrospectively registered
Titles & IDs
Public title
A Novel Liver Targeted Testosterone Therapy for Sarcopenia in Androgen Deprived Men with Prostate Cancer - A Blinded Randomized Controlled Trial
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Scientific title
A Novel Liver Targeted Testosterone Therapy for Sarcopenia in Androgen Deprived Men with Prostate Cancer - A Blinded Randomized Controlled Trial
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Secondary ID [1]
289807
0
nil known
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Universal Trial Number (UTN)
U1111-1185-9549
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Trial acronym
SADMCAP Trial
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Prostate Cancer
299727
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Sarcopenia
299728
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Androgen Deprivation Therapy
299729
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Condition category
Condition code
Metabolic and Endocrine
299661
299661
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0
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Other metabolic disorders
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Cancer
299662
299662
0
0
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Prostate
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Musculoskeletal
299825
299825
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0
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Other muscular and skeletal disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
40mg oral testosterone daily for 6 months
Will monitor adherence by patient log and drug packet return
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Intervention code [1]
295482
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Treatment: Drugs
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Comparator / control treatment
Placebo for 6 months - microcellulose
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Control group
Placebo
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Outcomes
Primary outcome [1]
299125
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Measure of lean body mass after 6 months enrolment
Aim for difference between treatment and placebo arms of 1.6kg at 80% power with 0.05 significance
Will assess using DEXA scan
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Assessment method [1]
299125
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Timepoint [1]
299125
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6 months post commencement of intervention
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Secondary outcome [1]
326251
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Prostate cancer progression
Assessed by PSA test
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Assessment method [1]
326251
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Timepoint [1]
326251
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6 months post commencement of intervention
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Eligibility
Key inclusion criteria
All men with prostate cancer on Androgen Deprivation therapy
- no time limit regarding diagnosis
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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
50% increase in PSA or increase in PSA to >4nmol/L above baseline after commencement of intervention
Previous Thyroid Dysfunction
Serious adverse event caused by product
Participants decision to withdrawl
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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)
Simple randomisation using block design
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 2
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
Proof of concept analysis
Assuming that treatment maintains LBM over 6 months, a sample size of 25 per group is required to achieve a significance difference 1.6kg LBM at 0.05 significance with 80% power between treatment and placebo. The present study sample size allows for a 10% drop out.
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
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Actual
8/08/2016
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Date of last participant enrolment
Anticipated
31/12/2017
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Actual
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Date of last data collection
Anticipated
30/06/2018
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Actual
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Sample size
Target
50
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Accrual to date
25
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Final
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Recruitment in Australia
Recruitment state(s)
QLD
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Recruitment hospital [1]
6343
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Princess Alexandra Hospital - Woolloongabba
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Recruitment hospital [2]
6344
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Greenslopes Private Hospital - Greenslopes
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Recruitment postcode(s) [1]
13885
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4102 - Woolloongabba
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Recruitment postcode(s) [2]
13886
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4120 - Greenslopes
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Funding & Sponsors
Funding source category [1]
294194
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Charities/Societies/Foundations
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Name [1]
294194
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Prostate Cancer Foundation Australia
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Address [1]
294194
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PO Box 499
St Leonards NSW 1590
Australia
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Country [1]
294194
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Australia
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Primary sponsor type
Hospital
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Name
Metro South Health and Hospital Service
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Address
Princess Alexandra Hospital
199 Ipswich Road, Woolloongabba, QLD 4102
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Country
Australia
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Secondary sponsor category [1]
293018
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Charities/Societies/Foundations
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Name [1]
293018
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Prostate Cancer Foundation Australia
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Address [1]
293018
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PO Box 499
St Leonards NSW 1590
Australia
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Country [1]
293018
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
295597
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Metro South HHS Human Research Ethics Committee
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Ethics committee address [1]
295597
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Metro South HHS Human Research Ethics Committee Princess Alexandra Hospital Ipswich Rd Wooloongabba QLD 4102
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Ethics committee country [1]
295597
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Australia
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Date submitted for ethics approval [1]
295597
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10/02/2016
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Approval date [1]
295597
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20/04/2016
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Ethics approval number [1]
295597
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HREC/16/QPAH/105
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Summary
Brief summary
The primary purpose of this trial is to evaluate the efficacy of oral testosterone for the prevention and treatment of sarcopenia in men with prostate cancer on Androgen Deprivation Therapy (ADT). Who is it for? You may be eligible to participate in this trial if you are aged 18 or over and have been diagnosed with prostate cancer, for which you are undergoing ADT. Study details All participants enrolled in this study will be randomly allocated (by chance) to receive either oral testosterone once per day for six months, or to receive an inactive sham tablet once per day for six months. All participants will be reviewed for sarcopenia by assessment of muscle mass with DEXA at six months, and for prostate cancer progression by PSA. It is hoped that the findings from this trial will provide information on the efficacy of oral testosterone for the prevention of sarcopenia in patients commencing ADT and the reversal of sarcopenia in patients on long term ADT, whilst evaluating whether this treatment has any impact on prostate cancer progression.
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Trial website
nil
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Trial related presentations / publications
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Public notes
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Attachments [1]
982
982
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0
/AnzctrAttachments/370868-2016_March_15 Ho PICF VERSION 2._KHdoc.doc
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Contacts
Principal investigator
Name
66530
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Prof Ken Ho
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Address
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c/o Maria Wojciechowski,
Project Officer & ESO to Professor Ken Ho & Paul Dall’Alba
Centres for Health Research Metro South Health
Level 7, Translational Research Institute, 37 Kent Street, WOOLLOONGABBA QLD 4102
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Country
66530
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Australia
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Phone
66530
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+61 7 34438066
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Fax
66530
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Email
66530
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[email protected]
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Contact person for public queries
Name
66531
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Ken Ho
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Address
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c/o Maria Wojciechowski, Project Officer & ESO to Professor Ken Ho & Paul Dall’Alba Centres for Health Research Metro South Health Level 7, Translational Research Institute, 37 Kent Street, WOOLLOONGABBA QLD 4102 a
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Country
66531
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Australia
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Phone
66531
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+61 7 34438066
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Fax
66531
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Email
66531
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[email protected]
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Contact person for scientific queries
Name
66532
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Ken Ho
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Address
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c/o Maria Wojciechowski, Project Officer & ESO to Professor Ken Ho, Centres for Health Research Metro South Health Level 7, Translational Research Institute, 37 Kent Street, WOOLLOONGABBA QLD 4102
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Country
66532
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Australia
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Phone
66532
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+61 7 34438066
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Fax
66532
0
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Email
66532
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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
A Novel Liver-Targeted Testosterone Therapy for Sarcopenia in Androgen Deprived Men with Prostate Cancer.
2021
https://dx.doi.org/10.1210/jendso/bvab116
N.B. These documents automatically identified may not have been verified by the study sponsor.
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