# Identification of the Molecular and/or Pathophysiological Bases of Rare Diseases of Genetic Origin (or Rare Forms of Frequent Diseases Suspected of Being of Genetic Origin).

> **NCT03287193** · — · RECRUITING · sponsor: **Centre Hospitalier Universitaire Dijon** · enrollment: 850 (estimated)

## Conditions studied

- Rare Diseases of Genetic Origin
- Rare Forms of Common Diseases Suspected of Being Genetic in Origin

## Interventions

- **BIOLOGICAL:** Blood and/or tissue sampling
- **GENETIC:** high-throughput sequencing

## Key facts

- **NCT ID:** NCT03287193
- **Lead sponsor:** Centre Hospitalier Universitaire Dijon
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** RECRUITING
- **Start date:** 2017-03-13
- **Primary completion:** 2027-03
- **Final completion:** 2027-12
- **Target enrollment:** 850 (ESTIMATED)
- **Last updated:** 2025-12-08


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03287193

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03287193, "Identification of the Molecular and/or Pathophysiological Bases of Rare Diseases of Genetic Origin (or Rare Forms of Frequent Diseases Suspected of Being of Genetic Origin).". Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/clinical/NCT03287193. Licensed CC0.

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