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Clinical Trials/NCT03889964
NCT03889964
Unknown
N/A

Reduced Exercise Capacity in Patients With Chronic Obstructive Pulmonary Disease -Relevance of Cardiovascular Comorbidities

Klinik für Kardiologie, Pneumologie und Angiologie1 site in 1 country100 target enrollmentMarch 1, 2019

Overview

Phase
N/A
Intervention
Not specified
Conditions
Chronic Obstructive Pulmonary Disease
Sponsor
Klinik für Kardiologie, Pneumologie und Angiologie
Enrollment
100
Locations
1
Primary Endpoint
Measurement of oxygen uptake during cardiopulmonary exercise testing (% predicted)
Last Updated
6 years ago

Overview

Brief Summary

In this study, cardiopulmonary exercise will be assessed to characterize the relevance of severity of COPD and coexisting cardiovascular comorbidities for exercise capacity.

Detailed Description

In patients with chronic obstructive pulmonary disease (COPD) the interpretation of dyspnoea also needs to consider coexisting cardiovascular disease. Cardiopulmonary exercise testing (CPET) is used to characterize pulmonary and cardiac function and limitations during exercise. The investigators hypothesise that cardiopulmonary exercise is reduced in COPD patients with coexisting cardiovascular disease as well as in more symptomatic patients and in patients with frequent exacerbations. For this purpose, 100 patients with with stable COPD are characterized by clinical characteristics, laboratory tests, lung function, electrocardiography, echocardiography and cardiopulmonary exercise testing.

Registry
clinicaltrials.gov
Start Date
March 1, 2019
End Date
December 2020
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Klinik für Kardiologie, Pneumologie und Angiologie
Responsible Party
Sponsor Investigator
Principal Investigator

Klinik für Kardiologie, Pneumologie und Angiologie

Principle Investigator

Heinrich-Heine University, Duesseldorf

Eligibility Criteria

Inclusion Criteria

  • patients with stable chronic obstructive pulmonary disease, exacerbated or stable
  • 40-80 years
  • sinus rhythm
  • informed written consent

Exclusion Criteria

  • Inability to give written consent
  • acute myocardial infarction with ST-segment elevations in last 30 days
  • severe acute or chronic renal dysfunction
  • severe heart failure-
  • atrial fibrillation
  • severe valve disease
  • severe hypoxemia
  • long term oxygen therapy or non invasive ventilation

Outcomes

Primary Outcomes

Measurement of oxygen uptake during cardiopulmonary exercise testing (% predicted)

Time Frame: Baseline

Secondary Outcomes

  • Measurement of Maximum wattage during cardiopulmonary exercise testing(Baseline)
  • Measurement of FEV1(Baseline)
  • Presence of cardiovascular comorbidities(Baseline)
  • N-terminal pro brain natriuretic peptid (NTproBNP) in ng/L from peripheral venous blood at baseline(Baseline)
  • measurement of dyspnoea quantified by the COPD assessment test as well as the modified Medical Research Council Scale(Baseline)
  • Measurement of Breathing reserve during cardiopulmonary exercise testing(Baseline)
  • Measurement of Oxygen pulse during cardiopulmonary exercise testing(Baseline)
  • Measurement the capillary pO2 in mmHg and capillary pCO2 at baseline(Baseline)

Study Sites (1)

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