# Integration of New Generation Multi-omics Analyses for the Diagnosis of Genetic Neurodevelomental Disorders

> **NCT07755098** · NA · NOT_YET_RECRUITING · sponsor: **Centre Hospitalier Universitaire Dijon** · enrollment: 132 (estimated)

## Conditions studied

- Intellectual Disability
- Neurodevelopmental Disorder (Diagnosis)
- srGS
- lrGS
- Short-read Genome Sequencing
- Long-read Genome Sequencing

## Interventions

- **DIAGNOSTIC_TEST:** Re-analysis of available srGS data
- **DIAGNOSTIC_TEST:** Re-analysis of available srGS data, followed by complementary analyses (lrGS sequencing, mRNA, and GMOs)
- **DIAGNOSTIC_TEST:** srGS sequencing
- **DIAGNOSTIC_TEST:** Short-read sequencing (srGS) followed by long-read sequencing (lrGS,), mRNA-sequencing and GMO testing

## Key facts

- **NCT ID:** NCT07755098
- **Lead sponsor:** Centre Hospitalier Universitaire Dijon
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** NOT_YET_RECRUITING
- **Start date:** 2026-09
- **Primary completion:** 2029-03
- **Final completion:** 2029-03
- **Target enrollment:** 132 (ESTIMATED)
- **Last updated:** 2026-08-10


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT07755098

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT07755098, "Integration of New Generation Multi-omics Analyses for the Diagnosis of Genetic Neurodevelomental Disorders". Retrieved via MORVS 2026-10-20 from https://api.morvs.ai/clinical/NCT07755098. Licensed CC0.

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