# Prevalence of POU4F3 and SLC17A8 Mutations

> **NCT01802190** · — · TERMINATED · sponsor: **University Hospital, Montpellier** · enrollment: 50 (actual)

## Conditions studied

- Familial Deafness

## Interventions

- **GENETIC:** Deafness patients

## Key facts

- **NCT ID:** NCT01802190
- **Lead sponsor:** University Hospital, Montpellier
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** TERMINATED
- **Start date:** 2011-03
- **Primary completion:** 2014-09
- **Final completion:** 2014-09
- **Target enrollment:** 50 (ACTUAL)
- **Why stopped:** No convincing results
- **Last updated:** 2015-07-21


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01802190

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01802190, "Prevalence of POU4F3 and SLC17A8 Mutations". Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/clinical/NCT01802190. Licensed CC0.

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