Follicle Stimulating Hormone (FSH) to Improve Testicular Development in Men With Hypogonadism (NCT00064987) | Clinical Trial Compass
TerminatedPhase 2
Follicle Stimulating Hormone (FSH) to Improve Testicular Development in Men With Hypogonadism
Stopped: Recruitment was at a standstill. We are currently preparing our results for publication.
United States19 participantsStarted 2001-04
Plain-language summary
Men with idiopathic hypogonadotropic hypogonadism (IHH, Kallmann Syndrome) may have small testicular size, low testosterone levels, no history of puberty, and infertility. These men lack a hormone called gonadotropin releasing hormone (GnRH) that stimulates the development and maturation of the testes. This study will investigate the impact of hormonal treatments on men with IHH. The goal of hormonal therapy is to maximize the potential fertility in these individuals.
Who can participate
Age range
18 Years
Sex
MALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria
* no history of spontaneous puberty
* clinical hypogonadism
* infantile testes (\< 3 ml)
* no reproductive hormone therapy except testosterone
* Complete absence of normal LH pulses during 12-hour baseline frequent blood sampling and serum testosterone \< 100 ng/dl
* Normal testing of the anterior pituitary gland
* Negative MRI of the hypothalamic-pituitary area
Exclusion Criteria
* Prior therapy with gonadotropins (FSH, hCG, or GnRH)
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
LH
Timeframe: month 4 of GnRH treatment
2
FSH
Timeframe: month 4 of GnRH treatment
3
Testosterone
Timeframe: month 4 of GnRH treatment
4
Inhibin B
Timeframe: month 4 of GnRH treatment
5
Testicular Size (Volume)
Timeframe: at baseline and month 4 of GnRH treatment
6
Sperm Count
Timeframe: month 4 of GnRH treatment
Trial details
NCT IDNCT00064987
SponsorEunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)