# Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions

> **NCT00758108** · — · COMPLETED · sponsor: **Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)** · enrollment: 197 (actual)

## Conditions studied

- WAGR Syndrome
- Wilm's Tumor
- Aniridia
- Urogenital Abnormalities
- Mental Retardation

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT00758108
- **Lead sponsor:** Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
- **Sponsor class:** NIH
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2008-09-11
- **Primary completion:** —
- **Final completion:** 2015-04-29
- **Target enrollment:** 197 (ACTUAL)
- **Last updated:** 2019-12-12


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00758108

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00758108, "Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions". Retrieved via AI Analytics 2026-07-19 from https://api.ai-analytics.org/clinical/NCT00758108. Licensed CC0.

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