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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00457912
Other study ID # IRB05-00101
Secondary ID NIH Grant U54AR0
Status Completed
Phase N/A
First received April 6, 2007
Last updated January 23, 2018
Start date June 2005
Est. completion date January 1, 2018

Study information

Verified date January 2018
Source Nationwide Children's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The objective of this study is to identify and maintain a registry of well-characterized limb-girdle muscular dystrophy (LGMD) patients. Patients seen as part of this study may be candidates for future treatment trials based on their defined genetic classification of LGMD. In the course of this study, the investigators will perform a muscle biopsy and DNA testing in an unlimited number of patients with clinically diagnosed LGMD. The genetic testing will be extended to the family of the study subject in order to better understand true genetic defect.


Recruitment information / eligibility

Status Completed
Enrollment 277
Est. completion date January 1, 2018
Est. primary completion date January 1, 2018
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- any subject with clinical diagnosis of LGMD

- must visit Columbus Children's Hospital for 2-day study visit

- muscle biopsy tissue must be available; either from previous biopsy, affected relative, or willing to have biopsy at Columbus Children's

Exclusion Criteria:

- diagnosis of a neuromuscular disorder other than LGMD

- unable to provide muscle tissue from previous or current biopsy

- incapable of giving consent and not having a legal guardian willing or able to do so

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Nationwide Children's Hospital Columbus Ohio

Sponsors (3)

Lead Sponsor Collaborator
Nationwide Children's Hospital Muscular Dystrophy Association, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

Country where clinical trial is conducted

United States, 

See also
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Terminated NCT03783923 - A Study of Deflazacort (Emflaza®) in Participants With Limb-Girdle Muscular Dystrophy 2I (LGMD2I) Phase 3
Completed NCT02635321 - MRI and Muscle Involvement in Patients With Mutations in GMPPB N/A
Completed NCT00873782 - Safety Study of Transvenous Limb Perfusion in Human Muscular Dystrophy Phase 1
Not yet recruiting NCT06399770 - The Role of Muscle Ultrasound in Assessment of Sample of Patients With Limb-girdle Muscular Dystrophy
Completed NCT04054375 - Weekly Steroids in Muscular Dystrophy Phase 2
Recruiting NCT00390104 - Molecular Analysis of Patients With Neuromuscular Disease
Recruiting NCT06246513 - A Trial to Learn More About an Experimental Gene Therapy Called Bidridistrogene Xeboparvovec (SRP-9003) as a Possible Treatment for Limb Girdle Muscular Dystrophy 2E/R4 (EMERGENE) Phase 3
Completed NCT00104078 - Study Evaluating MYO-029 in Adult Muscular Dystrophy Phase 1/Phase 2
Recruiting NCT04475926 - A Study of the Natural History of Participants With LGMD2E/R4, LGMD2D/R3, LGMD2C/R5, and LGMD2A/R1 ≥ 4 Years of Age, Who Are Managed in Routine Clinical Practice
Completed NCT02759302 - MRI on Persons With Mutations in POMT2 Gene (LGMD2N) N/A