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Decoding Central Defects in Dystrophinopathies From Diagnostic to Remediation

Name: Decoding Central Defects in Dystrophinopathies From Diagnostic to Remediation — clinical trial record (NCT07125898)
Creator: DataLookout
License: https://creativecommons.org/licenses/by/4.0/

Study acronym: DECODYS

StatusRecruiting

PhaseNot specified

SponsorAssistance Publique - Hôpitaux de Paris

Started2026-09-16

View on ClinicalTrials.gov ↗

Trial flagged as At Risk

Primary completion moved at least 11 months later Oct 1, 2027 → Sep 2028

See other at-risk trials from Assistance Publique - Hôpitaux de Paris

Amendment history

2026-09-23

Recruitment opened

Primary completion pushed: 2027-10-01 → 2028-09

Completion pushed: 2029-04-01 → 2031-03

Assistance Publique - Hôpitaux de Paris

1,338 trials monitored

See 38 trials at risk

The study aims to identify a genotype/phenotype correlation by analyzing more finely the neurodevelopmental disorders in DMD patients.

Trial Details

NCT Number	NCT07125898
Lead Sponsor	Assistance Publique - Hôpitaux de Paris
Conditions	Dystrophinopathies
Enrollment	110 participants
Start Date	2026-09-16
Primary Completion	2028-09 (estimated)
Study Completion	2031-03 (estimated)
Updated on ClinicalTrials.gov	2026-09-22