# Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions

> **NCT02077894** · — · RECRUITING · sponsor: **National Eye Institute (NEI)** · enrollment: 2000 (estimated)

## Conditions studied

- Genetic Eye Disease

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT02077894
- **Lead sponsor:** National Eye Institute (NEI)
- **Sponsor class:** NIH
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** RECRUITING
- **Start date:** 2014-08-05
- **Primary completion:** 2029-08-05
- **Final completion:** 2029-08-05
- **Target enrollment:** 2000 (ESTIMATED)
- **Last updated:** 2026-05-15


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02077894

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02077894, "Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions". Retrieved via AI Analytics 2026-07-18 from https://api.ai-analytics.org/clinical/NCT02077894. Licensed CC0.

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