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NCT04068961: GENALB

New Strategies of Genetic Study of Patients With Oculocutaneous Albinism

Completed Last updated 28 August 2019
What this trial tests

trial testing Genetic analyzes in Oculocutaneous Albinism in 64 participants. Completed in 31 October 2010.

Timeline
15 September 2010
Primary endpoint
31 October 2010
31 October 2010

Quick facts

Lead sponsorUniversity Hospital, Bordeaux
StatusCompleted
Study typeOBSERVATIONAL
Enrollment64
Start date15 September 2010
Primary completion31 October 2010
Estimated completion31 October 2010

Drugs / interventions tested

Conditions studied

Sponsor

University Hospital, Bordeaux

Who can join

Eligibility, any sex, with Oculocutaneous Albinism or Mutation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The oculocutaneous albinism is an autosomal recessive condition associated with mutations in 4 genes. In 20% of patients no mutation is identified. The optimization of genetic analysis methods and the search for new genes involved will help improve the diagnosis in these patients.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other University Hospital, Bordeaux trials

Trials by the same sponsor.

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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/NCT04068961.

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