ACTRN12609000462280CompletedPhase 4
A two part study to compare the pharmacological effects of recombinant human chorionic gonadotrophin (rhCG/Ovidrel) versus urinary human chorionic gonadotrophin (uhCG/Pregnyl) given as subcutaneous injection to healthy men following supression of endogenous testosterone (T) and luteinising hormone (LH) with nandrolone decanoate(ND).
Concord Repatriation General Hospital (CRGH)0 sites32 target enrollmentStarted: June 16, 2009Last updated:
Conditions
Trial Snapshot
- Phase
- Phase 4
- Status
- Completed
- Sponsor
- Enrollment
- 32
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
- Allocation
- Randomised controlled trial
- Primary Purpose
- Treatment
- Masking
- Open (masking not used)
Eligibility Criteria
- Ages
- 18 Years to o limit (—)
- Sex
- Male
Inclusion Criteria
- •Healthy men over 18 years of age
Exclusion Criteria
- •History of:
- •1. Chronic disease or condition requiring regular medical treatment,
- •2. Male infertility or pituitary-testicular dysfunction
- •3. Androgen (anabolic steriod) use or abuse
Investigators
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