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Detection of gonadotropin releasing hormone (GnRH) analogs as doping or masking agents

Detection of gonadotropin releasing hormone (GnRH) analogs as a sports doping agent in healthy male volunteers aged 18 to 50. An open label, randomised, placebo controlled clinical study.

Status
Not yet recruiting
Phases
Phase 3
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12609000189224
Enrollment
32
Registered
2009-04-17
Start date
2009-01-01
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Sports anti-doping study. The aim of this study is to see what effects on testosterone an injection of a synthetic hormone called GnRH analog has. GnRH analogs are banned in elite sports as they are considered to enhance an athletes performance by increasing the bodies production of testosterone. In this study blood and urine specimens will be collected from healthy male volunteers who have been given several injections a GnRH analog. Some of the volunteers will also be given an injection of testosterone or a drug called nandrolone. These three drugs are all banned in elite athletes, but it is thought that they may be being used in combination illicitly. Some of the volunteers will recieve injections of saline only given as a placebo, this allows us to compare the results with those of the volunteers receiving the drugs. The blood and urine samples taken from the volunteers (before and after the injections) will be analysed to see what effects they have on hormone levels, and will be used to help develop a test to detect the use of GnRH anaolgs by elite athletes.

Interventions

Particpants will be randomly allocated to one of four treatment groups. Group 1 will receive daily subcutaneous (s/c) injections of saline (placebo) for 4 days. Group 2 will receive daily s/c injections of superactive GnRH analog (Lucrin 1mg) for 4 days. Group 3 will receive daily s/c injections of Lucrin 1mg for 4 days and concurrent administration of 100mg injectable testosterone (T) esters to supress endogenous leutenising hormone (LH) and T production. Group 4 will receive daily s/c injecti

Particpants will be randomly allocated to one of four treatment groups. Group 1 will receive daily subcutaneous (s/c) injections of saline (placebo) for 4 days. Group 2 will receive daily s/c injections of superactive GnRH analog (Lucrin 1mg) for 4 days. Group 3 will receive daily s/c injections of Lucrin 1mg for 4 days and concurrent administration of 100mg injectable testosterone (T) esters to supress endogenous leutenising hormone (LH) and T production. Group 4 will receive daily s/c injections of Lucrin 1mg for 4 days and concurrent administration of nandrolone decanoate 100mg to supress endogenous LH and T production. Blood and urine samples will be collected from all particpants at intervals from 0 for up to 14 days.

Sponsors

Sydney South Western Area Health Service (SSWAHS)
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
Male
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

Healthy males

Exclusion criteria

Recent history of steroid use

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026