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Comparative Study of Clinical Endpoint in DMD: Handheld Myometry (HHM) Versus CINRG Quantitative Measurement System (CQMS)

NCT01125709 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2013-01-11

No results posted yet for this study

Summary

The aim of the proposed research is to compare two commonly used pediatric strength testing measures: handheld myometry (HHM) and CINRG Quantitative Measurement System (CQMS), with the goal of identifying a sensitive and valid tool for measuring muscle strength in children with DMD. The data obtained from this study will be used to make recommendations for strength measurement endpoints in prospective muscular dystrophy trials and provide more reliable and accurate recommendations in the clinic for strength assessment. This study will be performed at six participating sites in the Cooperative International Neuromuscular Research Group (CINRG).

Conditions

Sponsors & Collaborators

  • Muscular Dystrophy Association

    collaborator OTHER

  • Children's National Research Institute

    collaborator OTHER

  • Washington University School of Medicine

    collaborator OTHER

  • Royal Children's Hospital

    collaborator OTHER

  • Sydney Children's Hospitals Network

    collaborator OTHER

  • Fondazione Serena Onlus - Centro Clinico NeMO Milano

    collaborator OTHER

  • Carolinas Medical Center

    collaborator OTHER

  • Cooperative International Neuromuscular Research Group

    lead NETWORK

Principal Investigators

  • Tina T Duong, MPT · Children's National Research Institute

Eligibility

Min Age
6 Years
Max Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-01-31
Primary Completion
2010-06-30
Completion
2010-08-31

Countries

  • United States
  • Australia
  • Italy

Study Locations

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Diseases
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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01125709 on ClinicalTrials.gov