RecruitingNCT01601171
Genetics of Reproductive Disorders (Including Kallmann Syndrome) and Cleft Lip and/or Palate
Studying Rare male infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Centre Hospitalier Universitaire Vaudois
- Principal Investigator
- Nelly Pitteloud, M.D.Centre Hositalier Universitaire Vaudois (CHUV)
- Enrollment
- 2000 enrolled
- Eligibility
- All sexes
- Timeline
- 2012 – 2030
Study locations (1)
- Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Canton of Vaud, Switzerland
Collaborators
Swiss National Science Foundation
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT01601171 on ClinicalTrials.govOther trials for Rare male infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin
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