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NCT05657938

Evaluation of Home Based Assessments on Participants With DMD

Completed Last updated 14 August 2023
What this trial tests

trial testing Wearable Device in Duchenne Muscular Dystrophy in 17 participants. Completed in 4 April 2023.

Timeline
13 October 2022
Primary endpoint
4 April 2023
4 April 2023

Quick facts

Lead sponsorSolid Biosciences Inc.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment17
Start date13 October 2022
Primary completion4 April 2023
Estimated completion4 April 2023
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Solid Biosciences Inc. — full company profile →

Who can join

Adults 4 to 12, male only, with Duchenne Muscular Dystrophy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is designed to evaluate the feasibility, wearability and participant satisfaction of novel outcome assessment tools in DMD patients which are performed in the home environment.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Real-World Postural Transitions as Biomarkers of Functional Impairment in Duchenne Muscular Dystrophy.
    Gramling CJ, Kairamkonda DD, Marshall JL, Morris C, et al · · 2025 · PMID 40416999 · DOI 10.1159/000545617

Verify or expand the search:

Other trials of Wearable Device

Trials testing the same drug.

Other recruiting trials for Duchenne Muscular Dystrophy

Currently open trials in the same condition.

Other Solid Biosciences Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05657938.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing