Clinical Trials Directory

Trials / Recruiting

RecruitingNCT02069756

The Duchenne Registry

The Duchenne Registry: An International, Patient-Report Registry for Individuals With Duchenne and Becker Muscular Dystrophy (Member of TREAT-NMD Neuromuscular Network)

Status
Recruiting
Phase
Study type
Observational
Enrollment
10,000 (estimated)
Sponsor
The Duchenne Registry · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The Duchenne Registry is an online, patient-report registry for individuals with Duchenne and Becker muscular dystrophy and carrier females. The purpose of the Registry is to connect Duchenne and Becker patients with actively recruiting clinical trials and research studies, and to educate patients and families about Duchenne and Becker care and research. At the same time, The Duchenne Registry is a valuable resource for clinicians and researchers in academia and industry, allowing access to de-identified datasets provided by patients and their families-information that is vital to advances in the care and treatment of Duchenne. The Duchenne Registry is a member of the TREAT-NMD Neuromuscular Network.

Detailed description

The Duchenne Registry (previously DuchenneConnect) was created in 2007 by Parent Project Muscular Dystrophy (PPMD), with assistance from the NIH, the CDC, and Emory Genetics. In early 2011, PPMD alone began financing the registry's operation and maintenance, and is the sole guardian of The Duchenne Registry and its material. Questions may be addressed to the Duchenne Registry Coordinators at telephone 888-520-8675 or coordinator@duchenneregistry.org. The Duchenne Registry Coordinators are certified genetic counselors who are available to answer questions regarding the registration process, genetic testing and counseling, and clinical trials and research studies.

Conditions

Timeline

Start date
2007-10-01
Primary completion
2027-10-01
Completion
2047-10-01
First posted
2014-02-24
Last updated
2025-02-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02069756. Inclusion in this directory is not an endorsement.