Clinical Trial

Genetics of Reproductive Disorders (Including Kallmann Syndrome) and Cleft Lip and/or Palate

Recruiting
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Record status
This record was last updated June 21, 2022 (before its estimated March 2025 completion). Its status may not reflect the trial's current state.
Summary
The purpose of this study is to explore the genetic basis of reproductive disorders and cleft lip and/or palate.
Protocol Amendment History 7 amendments
This ClinicalTrials.gov record has been amended 7 times since 2012-05-16; most recent amendment 2022-06-17.
Trial Details
NCT Number NCT01601171
Lead Sponsor Centre Hospitalier Universitaire Vaudois
Collaborators: Swiss National Science Foundation
Conditions Kallmann Syndrome, Hypogonadotropic Hypogonadism, Hypothalamic Amenorrhea, Polycystic Ovarian Syndrome, Precocious Puberty, Cleft Lip and Palate, Cleft Palate, Cleft Lip
Enrollment 2,000 participants
Start Date 2012-03
Primary Completion 2025-03 (estimated)
Study Completion 2030-03 (estimated)
Updated on ClinicalTrials.gov 2022-06-21