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NCT02890472

Prenatal Examination of Deletion 22q11 Syndrome : Thymic Dysgenesis THYMI Study

Completed Last updated 27 January 2021
What this trial tests

trial in 22q11 Deletion Syndrome Di George Syndrome in 13 participants. Completed in 31 December 2020.

Timeline
1 October 2017
Primary endpoint
1 July 2020
31 December 2020

Quick facts

Lead sponsorCentre Hospitalier Universitaire de Nīmes
StatusCompleted
Study typeOBSERVATIONAL
Enrollment13
Start date1 October 2017
Primary completion1 July 2020
Estimated completion31 December 2020
Sites1 location across France

Conditions studied

Sponsor

Centre Hospitalier Universitaire de Nīmes

Who can join

18 and older, female only, with 22q11 Deletion Syndrome Di George Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

22q11.2 microdeletion seems the prenatally under-diagnosed . Indeed , there is a mismatch between the series on the heart rate of 22q11.2 antenatal 84% against 30% in the adult series despite a perinatal mortality of 16% suggesting opportunities for improvement in the prenatal diagnosis of fetus with a microdeletion 22q11.2 , especially without heart 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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Data sources for this page

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