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NCT03283852: FORDEV

Identifying New Genetic Causes to Development Disorders

Recruiting now Last updated 5 June 2024
What this trial tests

trial testing blood sample in Disorders of Sex Development in 1,100 participants. Currently enrolling.

Timeline
21 February 2017
Primary endpoint
21 February 2027
21 February 2027

Quick facts

Lead sponsorFondation Ophtalmologique Adolphe de Rothschild
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment1,100
Start date21 February 2017
Primary completion21 February 2027
Estimated completion21 February 2027
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Fondation Ophtalmologique Adolphe de Rothschild — full company profile →

Who can join

Eligibility, any sex, with Disorders of Sex Development or Growth Disorders. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Disorders of growth, puberty and sex development can have genetic causes. The exome analysis could detect new mutations responsible for these disorders and the frequency of these mutations in these disorders, their association with other malformations.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of blood sample

Trials testing the same drug.

Other recruiting trials for Disorders of Sex Development

Currently open trials in the same condition.

Other Fondation Ophtalmologique Adolphe de Rothschild trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03283852.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing