Clinical trial
Genetics and Psychopathology in the 22q11 Deletion Syndrome
NCT00161109 · UMC Utrecht, Other · Unknown status
Key facts
| NCT number | NCT00161109 |
|---|---|
| Title | Genetics and Psychopathology in the 22q11 Deletion Syndrome |
| Official title | Genetics and Psychopathology in the 22q11 Deletion Syndrome |
| Lead sponsor | UMC Utrecht, Other |
| Collaborators | Netherlands Brain Foundation Children's Hospital of Philadelphia |
| Status | Unknown status |
| Study type | Observational |
| Conditions | Chromosome 22q11.2 Deletion Syndrome |
| Enrollment | 175 |
| Start date | Oct 1, 2002 |
| Completion | Oct 1, 2012 |
| First posted | Sep 12, 2005 |
| Last update posted | Oct 13, 2006 |
| Countries | Netherlands, United States |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: