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NCT02890472
Prenatal Examination of Deletion 22q11 Syndrome : Thymic Dysgenesis THYMI Study
trial in 22q11 Deletion Syndrome Di George Syndrome in 13 participants. Completed in 31 December 2020.
1 July 2020
Quick facts
| Lead sponsor | Centre Hospitalier Universitaire de Nīmes |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 13 |
| Start date | 1 October 2017 |
| Primary completion | 1 July 2020 |
| Estimated completion | 31 December 2020 |
| Sites | 1 location across France |
Conditions studied
- 22q11 Deletion Syndrome Di George Syndrome — all drugs for 22q11 Deletion Syndrome Di George Syndrome →
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.
Verify or expand the search:
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT02890472 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Centre Hospitalier Universitaire de Nīmes
- Last refreshed: 27 January 2021
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/NCT02890472.
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