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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00295113
Other study ID # 2398
Secondary ID
Status Completed
Phase N/A
First received September 13, 2005
Last updated November 28, 2007
Start date November 2001
Est. completion date June 2003

Study information

Verified date November 2007
Source University Hospital, Strasbourg, France
Contact n/a
Is FDA regulated No
Health authority France: Ministry of Health
Study type Interventional

Clinical Trial Summary

The aim of the study is to observe the ventilatory and cardiac function (included the pulmonary arterial pressure) during an intermittent work exercise test with high density work load.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date June 2003
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- COPD patients (male and female) with moderate obstruction (FEV1/CV<60%)

Exclusion Criteria:

- acute respiratory disease

- any type of cardiac disease

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Procedure:
EFR


Locations

Country Name City State
France Hôpitaux Universitaires de Strasbourg - Service des Explorations Fonctionnelles Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary The pulmonary arterial pressure does not increase dramatically during the 30 minutes exercise test, but decreases significantly after the first 5 minutes of exercise.
Secondary The cardiac output is stable after the first 5 minutes of exercise, despite the high intensity work loads every 5 minutes.
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