# Phenotype Correlates Genotype of Inherited Retina Dystrophies, Retinitis Pigmentosa, Con>Rod Dystrophies.

> **NCT03990727** · — · UNKNOWN · sponsor: **MejoraVisionMD** · enrollment: 17000 (estimated)

## Conditions studied

- Retinitis Pigmentosa
- Cone Dystrophy
- Usher Syndromes
- Retina; Dystrophy

## Interventions

- **DIAGNOSTIC_TEST:** Retina Analysis-mosaic
- **DIAGNOSTIC_TEST:** Autofluorescence
- **DIAGNOSTIC_TEST:** OCT- 1 micra
- **PROCEDURE:** Genotype analysis

## Key facts

- **NCT ID:** NCT03990727
- **Lead sponsor:** MejoraVisionMD
- **Sponsor class:** NETWORK
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2009-08
- **Primary completion:** 2019-06-13
- **Final completion:** 2025-09-30
- **Target enrollment:** 17000 (ESTIMATED)
- **Last updated:** 2019-06-19

## Collaborators

- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03990727

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03990727, "Phenotype Correlates Genotype of Inherited Retina Dystrophies, Retinitis Pigmentosa, Con>Rod Dystrophies.". Retrieved via AI Analytics 2026-06-03 from https://api.ai-analytics.org/clinical/NCT03990727. Licensed CC0.

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