Muscle Atrophy In Patients With Chronic Obstructive Pulmonary Disease

NCT ID: NCT02284932

Last Updated: 2016-09-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

36 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-09-30

Study Completion Date

2018-09-30

Brief Summary

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Limb muscle dysfunction, characterized by atrophy and weakness, is amongst the most troublesome systemic consequences of chronic obstructive pulmonary disease (COPD) leading to poor functional status and premature mortality.

One prevailing hypothesis stipulates that the deterioration in muscle structure and function during COPD results from a spillover of inflammatory mediators from the lungs to the systemic circulation and then to the muscles.

Detailed Description

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The investigators objective is to investigate the impact of COPD on key signaling pathways involved in the muscle atrophy. Moderate to severe COPD patients (FEV1 under 60% of predicted) and healthy controls will be recruited. All of the investigators patients will undergo a thorough baseline assessment in pulmonary capacity, muscle force and body composition. Blood sampling and biopsy of the quadriceps will be done. Key proteins of signaling intramuscular pathways involved in protein synthesis and degradation will be measured in the quadriceps.

Conditions

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Chronic Obstructive Pulmonary Disease

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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COPD patients

Group : COPD patients No specific intervention for this study

No specific intervention for this study

Intervention Type OTHER

No specific intervention for this study

Healthy controls

Group : healthy volunteers No specific intervention for this study

No specific intervention for this study

Intervention Type OTHER

No specific intervention for this study

Interventions

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No specific intervention for this study

No specific intervention for this study

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* male
* COPD with an FEV1 of under 60% of predicted
* non-smoker
* between 55 and 75 years old

Exclusion Criteria

* all inflammatory disease (HIV, cancer, renal and cardiac deficiency)
* hormonal dysregulation
* inferior limb pathology
* neuromuscular pathology
* history of tobacco or alcool abuse
* oxygen dependent
* recent exacerbation (2 months) of the symptoms of COPD
Minimum Eligible Age

55 Years

Maximum Eligible Age

75 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

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Canadian Institutes of Health Research (CIHR)

OTHER_GOV

Sponsor Role collaborator

Laval University

OTHER

Sponsor Role lead

Responsible Party

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Annie Dubé

Professionelle de recherche

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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François Maltais, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Institut universitaire de cardiologie et de pneumologie de Québec, University Laval

Locations

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Centre de recherche de l'Institut universitaire de cardiologie et de pneumologie de Québec

Québec, Quebec, Canada

Site Status

Countries

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Canada

Other Identifiers

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COPD-20739

Identifier Type: -

Identifier Source: org_study_id

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