Clin2
NCT01500447Possibly a fitRecruiting

Study of inherited causes of low puberty hormones

Genetic DisorderInfertilityHypogonadismAmenorrhea

Part of Genetic & congenital, Hormones & metabolism, Kidney & urinary, Women’s health & pregnancy clinical trials.

This study looks at families to understand inherited (genetic or family-related) reasons some people have delayed puberty or develop puberty abnormally. It may help doctors better figure out the cause of low sex hormone levels and related hormone problems.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
850 people
Ages
1 month to 120 years
Study type
Observational

Who can take part

  • You have puberty that is delayed, too early, or later followed by low sex hormone levels
  • OR your clinician suspects an increased risk of hypogonadotropic hypogonadism (low puberty-driving signals from the brain)
  • Your sex hormone pattern is consistent with low sex steroids and low or normal “gonadotropins” (measured blood hormone levels)
  • You do not have additional pituitary hormone deficiencies beyond the suspected puberty signal issue
  • You are not taking medicines that can affect the brain’s puberty hormone signals (such as long-term corticosteroids or continuous opioid use)

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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