# Diagnostic Research in Patients With Rare Diseases - Solving the Unsolved Rare Diseases

> **NCT03491280** · — · UNKNOWN · sponsor: **University Hospital Tuebingen** · enrollment: 5500 (estimated)

## Conditions studied

- Rare Diseases
- Genetic Predisposition

## Interventions

- **GENETIC:** NGS Diagnostic

## Key facts

- **NCT ID:** NCT03491280
- **Lead sponsor:** University Hospital Tuebingen
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2018-05-01
- **Primary completion:** 2023-04
- **Final completion:** 2025-04
- **Target enrollment:** 5500 (ESTIMATED)
- **Last updated:** 2022-05-23


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03491280

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03491280, "Diagnostic Research in Patients With Rare Diseases - Solving the Unsolved Rare Diseases". Retrieved via AI Analytics 2026-06-05 from https://api.ai-analytics.org/clinical/NCT03491280. Licensed CC0.

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