# Genetics and Psychopathology in the 22q11 Deletion Syndrome

> **NCT00161109** · — · UNKNOWN · sponsor: **UMC Utrecht** · enrollment: 175 (—)

## Conditions studied

- Chromosome 22q11.2 Deletion Syndrome

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT00161109
- **Lead sponsor:** UMC Utrecht
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2002-10
- **Primary completion:** —
- **Final completion:** 2012-10
- **Target enrollment:** 175 (—)
- **Last updated:** 2006-10-13

## Collaborators

- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00161109

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00161109, "Genetics and Psychopathology in the 22q11 Deletion Syndrome". Retrieved via AI Analytics 2026-06-24 from https://api.ai-analytics.org/clinical/NCT00161109. Licensed CC0.

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