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NCT03065686: GENEPIC

Identification of Genetic Factors Implicated in Orofacial Cleft Using Whole Exome Sequencing

Status unknown NA Last updated 10 February 2023
What this trial tests

NA trial testing identification of genetic factors in Cleft Lip and Palate in 30 participants. Status unknown.

Timeline
30 November 2016
Primary endpoint
30 November 2023
30 November 2023

Quick facts

Lead sponsorCentre Hospitalier Universitaire, Amiens
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposebasic science
Enrollment30
Start date30 November 2016
Primary completion30 November 2023
Estimated completion30 November 2023
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Centre Hospitalier Universitaire, Amiens

Who can join

Eligibility, any sex, with Cleft Lip and Palate. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Despite significant progress made in identification on numerous genes and gene pathways critical for craniofacial development, several approaches, ie mutation screening of specific candidates, association studies and even genome-wide scans have largely failed to reveal the molecular basis of NS human clefting

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Cleft Lip and Palate

Currently open trials in the same condition.

Other Centre Hospitalier Universitaire, Amiens 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/NCT03065686.

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