Plain-English translation of NCT00250159 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This is a long-term observational study that follows patients with two genetic conditions that cause excess male hormones in childhood: Congenital Adrenal Hyperplasia (CAH) and Familial Male-Limited Precocious Puberty (FMPP). Researchers are collecting detailed information about how these conditions affect growth, development, metabolism, and psychological well-being over time. The study is not testing a new medication, but rather tracking patients to better understand these rare conditions and improve future treatments.
Children with excess male hormones often experience early puberty, accelerated growth, and shorter adult height, but doctors don't fully understand all the ways these conditions affect a patient's body and mind. This study aims to create a comprehensive picture of how these genetic disorders develop and progress, which will help doctors design better treatments in the future.
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Your participation will involve visiting the research clinic or working with your home doctor to provide medical information and allow researchers to collect blood samples and track your growth, development, and hormone levels. Some participants will be managed directly at the National Institutes of Health, while others will participate through their local physicians. The study is ongoing with no set end date, meaning you would be followed over months or years to help doctors understand how these conditions change over time.
AI-generated summary from trial data · Aug 20, 2026 · Not medical advice
United States