MedTrace Logo

Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders

NCT00494169 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 4042

Last updated 2022-06-30

No results posted yet for this study

Summary

The aims of this study are: 1) to identify genes that play a role in human pubertal development and reproduction, 2) to characterize the phenotypic spectrum of patients with these gene defects, and 3) to discern the mode of inheritance for disorders caused by these gene defects. We are specifically interested in genes that cause Kallmann syndrome, idiopathic hypogonadotropic hypogonadism (IHH), precocious (early) puberty, and delayed puberty. Individuals do not have to travel to Boston to participate in this study.

Conditions

  • Hypogonadotropic Hypogonadism
  • Kallmann Syndrome
  • Puberty, Delayed
  • Puberty, Precocious
  • GnRH Deficiency

Sponsors & Collaborators

  • Massachusetts General Hospital

    lead OTHER

Principal Investigators

  • Stephanie B Seminara, MD · Massachusetts General Hospital

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
1999-01-31
Primary Completion
2022-02-28
Completion
2022-02-28

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00494169 on ClinicalTrials.gov