RecruitingNCT03283852
Identifying New Genetic Causes to Development Disorders
Studying Syndrome with 46,XX difference of sex development
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
- Fondation Ophtalmologique Adolphe de Rothschild
- Principal Investigator
- Raja Brauner, PU-PHHôpital Fondation A. de Rothschild
- Intervention
- blood sample(genetic)
- Enrollment
- 1100 enrolled
- Eligibility
- All sexes
- Timeline
- 2017 – 2027
Study locations (1)
- Hôpital Fondation A de Rothschild, Paris, France
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 NCT03283852 on ClinicalTrials.govOther trials for Syndrome with 46,XX difference of sex development
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