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NCT00340626

Genetic Analysis of Hereditary Non-Syndromic Oral Clefts

Completed Last updated 13 March 2020
What this trial tests

trial in Hereditary Oral Clefts in 690 participants. Completed in 12 March 2020.

Timeline
31 August 1997
Primary endpoint
12 March 2020
12 March 2020

Quick facts

Lead sponsorNational Human Genome Research Institute (NHGRI)
StatusCompleted
Study typeOBSERVATIONAL
Enrollment690
Start date31 August 1997
Primary completion12 March 2020
Estimated completion12 March 2020
Sites1 location across Syria

Conditions studied

Sponsor

National Human Genome Research Institute (NHGRI)

Who can join

Eligibility, any sex, with Hereditary Oral Clefts. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In a collaborative effort with the IBN AL-NAFEES Hospital (Damascus, Syrian Arab Republic), individuals from multiplex families determined to have hereditary oral clefts will be studied. The purpose of this study is to identify the gene(s) involved in heritable oral clefts by linkage analysis and gene mapping strategies. Characterization of genes involved in inherited oral clefts could provide important insight into the inheritance and pathogenesis of this disease.

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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Trials by the same sponsor.

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