# Study of the Diagnostic Value of "Rapid" High Throughput Genome Sequencing Analysis in Diagnostic Emergency Situations

> **NCT03956069** · — · COMPLETED · sponsor: **Centre Hospitalier Universitaire Dijon** · enrollment: 57 (actual)

## Conditions studied

- Developmental Anomalies

## Interventions

- **BIOLOGICAL:** blood sample
- **GENETIC:** genome sequencing

## Key facts

- **NCT ID:** NCT03956069
- **Lead sponsor:** Centre Hospitalier Universitaire Dijon
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2020-06-23
- **Primary completion:** 2022-01-25
- **Final completion:** 2022-07-25
- **Target enrollment:** 57 (ACTUAL)
- **Last updated:** 2022-09-21


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03956069

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03956069, "Study of the Diagnostic Value of "Rapid" High Throughput Genome Sequencing Analysis in Diagnostic Emergency Situations". Retrieved via AI Analytics 2026-07-19 from https://api.ai-analytics.org/clinical/NCT03956069. Licensed CC0.

---

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