# Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases

> **NCT02309866** · — · UNKNOWN · sponsor: **Hillel Yaffe Medical Center** · enrollment: 100 (estimated)

## Conditions studied

- Retinitis Pigmentosa

## Interventions

- **GENETIC:** Genetic testing

## Key facts

- **NCT ID:** NCT02309866
- **Lead sponsor:** Hillel Yaffe Medical Center
- **Sponsor class:** OTHER_GOV
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2015-01
- **Primary completion:** 2017-01
- **Final completion:** 2018-01
- **Target enrollment:** 100 (ESTIMATED)
- **Last updated:** 2014-12-05

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02309866

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02309866, "Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT02309866. Licensed CC0.

---

*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*