The Molecular Basis of Inherited Reproductive Disorders (NCT05971836) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
The Molecular Basis of Inherited Reproductive Disorders
United States600 participantsStarted 2021-01-21
Plain-language summary
The goal of this study is to learn more about the genes that control puberty and reproduction in humans.
Who can participate
Age range1 Year
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Participants must belong to one of the following categories:
* Failure to go through a normal, age-appropriate, spontaneous puberty and low sex steroid levels in the setting of low/normal gonadotropins or,
* Abnormally early development of puberty or,
* Normal puberty with subsequent development of low gonadotropin levels or,
* Evidence of a reproductive disorder with high gonadotropin levels or,
* Pre-pubertal individuals with features suggestive of hypogonadotropic hypogonadism or,
* Affected and unaffected family members of individuals that fit criteria above