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Completed

NCT Number: NCT01066455

Cardiac Outcome Measures in Children With Muscular Dystrophy

The purpose of the research study is to evaluate different cardiac measures that are obtained by echocardiographic tests in patients with muscular dystrophy.

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Key information

About this study

The research study will include 50 participants aged 8 to 18 years old (before 18th birthday) with Duchenne, Becker, or autosomal recessive limb-girdle (specifically: LGMD 2C-2F and 2I) muscular dystrophies.

Participants will be seen in one of five Cooperative International Neuromuscular Research Group (CINRG) centers located in the United States.

All study assessments will be completed in the same day and include reviewing past medical and surgical history, collecting vital signs, collecting cardiac measures through echocardiographic tests.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants must be between the ages of 8 and 18 years old
  • Confirmed diagnosis of muscular dystrophy (DMD, BMD, or LGMD 2C-2F and 2I)

Exclusion criteria

  • Investigator assessment of inability to comply with protocol
  • History of a congenital cardiac defect or other cardiac disease unrelated to muscular dystrophy

Sponsors and collaborators

Lead sponsor

Cooperative International Neuromuscular Research Group

Network

Collaborators

  • National Institutes of Health (NIH)

Registry information

Official study title

PITT1109: Cardiac Outcome Measures in Children With Muscular Dystrophy

Important dates

Study start
2010
Primary completion
2012
Study completion
2012
First posted
Feb 10, 2010
Registry last updated
Jan 11, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Recruiting

The Duchenne Registry

NCT02069756

Becker Muscular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Washington D.C., District of Columbia, United States

View Trial Details