# Registry for Patients With Wilms' Tumor Suppressor Gene 1 (WT1) Mutation Associated Diseases

> **NCT01252901** · — · COMPLETED · sponsor: **Universitätsklinikum Hamburg-Eppendorf** · enrollment: 52 (actual)

## Conditions studied

- Denys-Drash Syndrome
- Frasier Syndrome
- Nephrotic Syndrome
- Wilms Tumor

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT01252901
- **Lead sponsor:** Universitätsklinikum Hamburg-Eppendorf
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2010-10
- **Primary completion:** 2013-11
- **Final completion:** 2014-06
- **Target enrollment:** 52 (ACTUAL)
- **Last updated:** 2015-05-28


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01252901

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01252901, "Registry for Patients With Wilms' Tumor Suppressor Gene 1 (WT1) Mutation Associated Diseases". Retrieved via AI Analytics 2026-06-03 from https://api.ai-analytics.org/clinical/NCT01252901. Licensed CC0.

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