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Trial registered on ANZCTR
Registration number
ACTRN12605000283673
Ethics application status
Approved
Date submitted
31/08/2005
Date registered
2/09/2005
Date last updated
29/02/2008
Type of registration
Prospectively registered
Titles & IDs
Public title
Testosterone in Obese Men Trial
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Scientific title
A 12-month Randomised, Placebo-controlled Trial of Testosterone Replacement Therapy and Lifestyle Modification Versus Lifestyle Modification Alone on Visceral Adiposity and Markers of Cardiovascular Risk in Obese Middle-Aged and Older Men
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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:
Obese Middle-Aged and Older Men with Borderline Androgen Deficiency
371
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Testosterone deficiency in ageing males
2893
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Condition category
Condition code
Diet and Nutrition
436
436
0
0
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Obesity
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Metabolic and Endocrine
437
437
0
0
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Other metabolic and endocrine disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
12-month Randomised, Placebo-controlled Trial of Testosterone Replacement Therapy (Intramuscular Testosterone Undecanoate) and Lifestyle Modification.
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Intervention code [1]
320
0
Treatment: Drugs
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Comparator / control treatment
Lifestyle Modification Alone
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Control group
Placebo
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Outcomes
Primary outcome [1]
498
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Change in visceral fat
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Assessment method [1]
498
0
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Timepoint [1]
498
0
After 52 weeks of intervention
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Secondary outcome [1]
1070
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Change in visceral fat
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Assessment method [1]
1070
0
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Timepoint [1]
1070
0
After 52 weeks of intervention
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Secondary outcome [2]
1071
0
Body Composition (Total Body Fat Mass and Fat Free Mass)
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Assessment method [2]
1071
0
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Timepoint [2]
1071
0
At 0 and 52 weeks
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Secondary outcome [3]
1072
0
Vascular Function (Pulse Wave Velocity)
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Assessment method [3]
1072
0
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Timepoint [3]
1072
0
At 0 and 52 weeks
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Secondary outcome [4]
1073
0
Metabolic (Insulin Resistance and Lipid Profiles)
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Assessment method [4]
1073
0
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Timepoint [4]
1073
0
At 0, 26 and 52 weeks
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Secondary outcome [5]
1074
0
Coagulation profiles
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Assessment method [5]
1074
0
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Timepoint [5]
1074
0
At 0, 6, 26, and 52 weeks.
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Eligibility
Key inclusion criteria
BMI between 30-39.9 kg/m2 and WC equal to or greater than102cm, Serum total Testosterone <12nM.
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Minimum age
40
Years
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Maximum age
70
Years
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Sex
Males
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Can healthy volunteers participate?
No
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Key exclusion criteria
Smokers, Significant medical condition, Sleep Apnoea, Contra-indications to Testosterone therapy.
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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)
Sealed envelopes provided by study drug manufacturer
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer generated sequence (by study drug manufacturer)
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Masking / blinding
Blinded (masking 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 3 / 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
Recruiting
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Date of first participant enrolment
Anticipated
1/12/2005
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
40
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
488
0
Other
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Name [1]
488
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PHIMR
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Address [1]
488
0
Prince Henry's Institute. Level 3, Block E, Monash Medical Centre, 246 Clayton Road, Clayton, Victoria, 3168
PO Box 5152, Clayton, Vic 3168
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Country [1]
488
0
Australia
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Funding source category [2]
489
0
Commercial sector/Industry
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Name [2]
489
0
Schering AG
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Address [2]
489
0
Schering Pty Ltd, 875 Pacific Highway, Pymble, NSW, 2073
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Country [2]
489
0
Australia
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Primary sponsor type
Government body
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Name
PHIMR
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Address
Prince Henry's Institute. Level 3, Block E, Monash Medical Centre, 246 Clayton Road, Clayton, Victoria, 3168
Po Box 5152, Clayton, Vic, 3168
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Country
Australia
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Secondary sponsor category [1]
393
0
None
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Name [1]
393
0
Nil
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Address [1]
393
0
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Country [1]
393
0
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Ethics approval
Ethics application status
Approved
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Summary
Brief summary
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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
35708
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Address
35708
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Country
35708
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Phone
35708
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Fax
35708
0
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Email
35708
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Contact person for public queries
Name
9509
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Sr. Elise Forbes
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Address
9509
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Prince Henry's Institute of Medical Research
Monash Medical Centre
Level 3 Block E
246 Clayton Road
Clayton VIC 3168
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Country
9509
0
Australia
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Phone
9509
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+ 61 3 95943554
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Fax
9509
0
+ 61 3 95943558
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Email
9509
0
[email protected]
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Contact person for scientific queries
Name
437
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Dr. Carolyn Allan
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Address
437
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Prince Henry's Institute of Medical Research
Monash Medical Centre
Level 3 Block E
246 Clayton Road
Clayton VIC 3168
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Country
437
0
Australia
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Phone
437
0
+ 61 3 95943004
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Fax
437
0
+ 61 3 95943558
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Email
437
0
[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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