# NIPD on cffDNA for Triplet Repeat Diseases

> **NCT04698551** · — · UNKNOWN · sponsor: **University Hospital, Montpellier** · enrollment: 36 (estimated)

## Conditions studied

- Myotonic Dystrophy 1
- Huntington Disease
- Fragile X Syndrome

## Interventions

- **GENETIC:** Non invasive prenatal diagnosis

## Key facts

- **NCT ID:** NCT04698551
- **Lead sponsor:** University Hospital, Montpellier
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2020-09-01
- **Primary completion:** 2023-09-01
- **Final completion:** 2023-12-01
- **Target enrollment:** 36 (ESTIMATED)
- **Last updated:** 2021-01-07

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04698551

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04698551, "NIPD on cffDNA for Triplet Repeat Diseases". Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/clinical/NCT04698551. Licensed CC0.

---

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