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OpenTrials
Completed

NCT Number: NCT04349566

Fast Troponin as a Biomarker to Assess Exercise-induced Muscle Damage in Muscle Diseases

The purpose of the study is to explore the biomarker Fast Troponins response to exercise in patients with Becker muscular dystrophy, Limb-girdle muscular dystrophy and McArdle disease

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Key information

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • The ability to cycle
  • No concurrent medical condition that could interfere with interpretation of the results
  • Molecular diagnosis of the specific condition in specified patient groups or healthy control
  • No active muscle injury on the test day (caused by recent exercise, seizures, trauma, etc.)

Exclusion criteria

  • Competing conditions at risk of compromising the results of the study
  • Cardiac or pulmonary disease contraindicating peak exercise testing or strenuous exercise
  • Veins that are too difficult to puncture for blood sampling, evaluated by the investigator
  • Severe muscle weakness, that prevents the subject completing the exercise test, evaluated by the investigator

Treatment and study plan

Primary outcomes

  1. Change in biomarkers

    Time frame: 24 hours

    Change in Fast and slow Troponin I after muscle damage

Sponsors and collaborators

Lead sponsor

Mads Peter Godtfeldt Stemmerik

Other

Collaborators

  • Edgewise Therapeutics, Inc.

Registry information

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Apr 16, 2020
Registry last updated
Oct 27, 2022

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.

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