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OpenTrials
Completed

NCT Number: NCT03028532

Administration of Clomiphene: Short and Long Term Metabolism in an Anti-Doping Setting

Clomiphene (Clomid) is a drug FDA approved to treat female infertility, however, it is often used by men in an off-label setting to both treat male infertility and in a multitude of sports disciplines to increase performance.

Study Objectives:

* Determine detection windows for clomiphene and its metabolites in urine following a medium-term administration * Understand the effect of clomiphene administration on luteinizing hormone (LH), follicle-stimulating hormone (FSH), and serum testosterone (T) concentrations in a longitudinal manner * Identify changes in current steroidal module of Athlete Biological Passport

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Key information

Age range

18 year–40 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

Heidi Jo Hansen

Salt Lake City, Utah, 84124, United States

About this study

Clomiphene, pharmaceutically prepared as clomiphene citrate, is a selective estrogen receptor modulator (SERM) with a therapeutic indication to treat female infertility. Though FDA-approved only for use in women, clomiphene is often prescribed off-label to males to treat male infertility and secondary hypogonadism due to its ability to increase serum testosterone levels. Numerous clinical studies have documented both the effectiveness for these indications and safety of clomiphene administration in males. Increasing the concentration of circulating testosterone can have additional effects, including the enhancement of performance in sports. As such, clomiphene is already abused by athletes in several sporting disciplines, including mixed martial arts, cycling, and bodybuilding. Therefore, clomiphene is a prohibited substance under the World Anti-Doping Agency code . Though the parent compound and metabolites of clomiphene are directly detectable in routine anti-doping screening, the urinary detection window and the effect of clomiphene administration on other anti-doping markers are unknown and thus the foci of this study.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Active males who engage in regular exercise between the ages of 18 and 40 on the day of enrollment
  • For this study, regular exercise is defined as: physical activity resulting in an increased heart rate for at least 30 minutes per day, 4-5 days per week.

Exclusion criteria

  • Individuals outside of the described age range on the day of enrollment
  • Individuals who are in a Registered Testing Pool for anti-doping purposes, or individuals who for any reason could be subject to doping control testing
  • Individuals who are unwilling or unable to provide blood or urine samples
  • Individuals who do not actively exercise
  • Individuals with any history of cancer, cardiovascular disease, endocrine abnormalities, infertility, hypoandrogenism, renal disease, hepatic disease, neurologic disease, or any psychiatric history
  • Individuals who have previously used anabolic steroids, selective estrogen receptor modulators (SERMs), selective androgen receptor modulators (SARMs), or who are currently using any substances included on the WADA Prohibited List
  • History of venous thromboembolic disease (i.e. deep vein thrombosis or pulmonary embolism)
  • History of untreated cataracts
  • History of intracranial lesions such as pituitary tumors
  • Transaminase elevation greater than 3 times the upper limit of normal (ULN)
  • Moderate or heavy alcohol intake

Treatment and study plan

Clomid

Drug

Participants will self-administer Clomid (50mg oral tablet) once daily for 30 consecutive days

Other names: Clomiphene, Clomifene

Primary outcomes

  1. The window of detection for the clomiphene parent compound and metabolites following a 30-day administration will be identified.

    Time frame: Day 30 through end of study participation (minimum, Day 72)

    ◦This will be determined as the amount of time following the final dose (day 30) until clomiphene nor its metabolites are no longer detectable in a urine sample.

Secondary outcomes

  1. Effect of clomiphene administration on serum LH, FSH, and T levels for potential inclusion into a hematological-based longitudinal steroid profile.

    Time frame: Day 30 through end of study participation (minimum, Day 72)

    A baseline for LH, FSH, and T will be established using the average of serum concentrations calculated from the pre-administration samples from each subject.The change in serum concentrations following administration will be compared against the baseline values.

  2. Effect on current steroidal module of Athlete Biological Passport

    Time frame: Day 30 through end of study participation (minimum, Day 72)

    ◦The steroidal module of the Athlete Biological Passport, a statistical model used to identify doping, will be used for data analysis in this study.As stated in the ABP Operating Guidelines, the steroidal compounds described above are considered for the ABP steroidal module in addition to the following ratios: T/E, A/T, A/Etio, 5aAdiol/5βAdiol, and 5aAdiol/E. Changes in the urinary steroid concentrations and these ratios will be assessed over the course of the study.

Sponsors and collaborators

Lead sponsor

Stuart Willick

Other

Collaborators

  • Partnership for Clean Competition
  • Sports Medicine Research and Testing Laboratory

Registry information

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Jan 23, 2017
Registry last updated
Jan 30, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.