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Clinical Trials/NCT00213850
NCT00213850CompletedNot Applicable

Reference Values for Respiratory Resistance Measured by the Interrupter Technique in Adults

University Hospital, Strasbourg, France2 sites in 1 country122 target enrollmentStarted: January 1, 2002Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
122
Locations
2
Primary Endpoint
References values obtained once

Study Overview

Brief Summary

The purpose is to obtain reference values of respiratory resistance (a technique widely used in children), in adults. The interest is that this technique needs only little co-operation and would be particularly adapted in subjects in whom co-operation is insufficient for other measurements.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Single Group
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Adult non smokers, without any disease interfering with pulmonary function

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

References values obtained once

Secondary Outcomes

  • Estimation of short-term reproductibility

Investigators

Sponsor
University Hospital, Strasbourg, France
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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