Substudy : Patients With an Acute Exacerbation of Chronic Obstructive Pulmonary Disease

NCT ID: NCT02282436

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

20 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-05-31

Study Completion Date

2018-05-31

Brief Summary

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Chronic obstructive pulmonary disease (COPD) is a leading cause of morbidity and mortality worldwide. Its prevalence is in progression and COPD is expected to become the fourth leading cause of death by 2030. COPD is characterized by periods of stability interspersed with acute infectious/inflammatory flare-ups, also called acute exacerbations, during which patients deteriorate, sometimes to the point of requiring immediate medical assistance. Although most patients eventually recover, repeated episodes of exacerbations may accelerate COPD progression. Exacerbations may further compromise the integrity of limb muscles by promoting further loss in muscle mass and strength.

The overall objective of this substudy is to elucidate how an acute COPD exacerbation may affect limb muscles.

Detailed Description

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Focusing our attention during exacerbations, a period of aggravated systemic inflammation, should be more rewarding in terms of understanding the link between inflammation burst and muscle disease in COPD. We have recently acquired experimental data supporting a role for the ubiquitin proteasome pathway in the worsening of limb muscle structure and function during an acute exacerbation, providing a solid framework for this investigation. The overall objective of this proposal is to substantiate these preliminary findings and elucidate how systemic inflammation during acute COPD exacerbation may affect limb muscles. Ultimately, our research could open new therapeutic avenues to minimize the systemic consequences of an acute exacerbation.

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 exacerbation

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 and female
* COPD with an FEV1 of under 60% of predicted
* non-smoker
* between 50 and 75 years old
* experiencing an acute exacerbation of COPD (24-48 hours, before treatment)

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
Minimum Eligible Age

50 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

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

Professionnelle 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 de cardiologie et de pneumologie de Québec

Québec, Quebec, Canada

Site Status RECRUITING

Countries

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Canada

Central Contacts

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Annie Dubé, PhD

Role: CONTACT

418-656-8711 ext. 2673

Facility Contacts

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Annie Dubé, PhD

Role: primary

418-656-8711 ext. 2673

Other Identifiers

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EXA-COPD-20765

Identifier Type: -

Identifier Source: org_study_id

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