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

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00213850
First Posted: September 21, 2005
Last Update Posted: November 29, 2007
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
University Hospital, Strasbourg, France
  Purpose
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.

Condition Intervention
Healthy Procedure: EFR

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Official Title: Reference Values for Respiratory Resistance Measured by the Interrupter Technique in Adults

Further study details as provided by University Hospital, Strasbourg, France:

Primary Outcome Measures:
  • References values obtained once

Secondary Outcome Measures:
  • Estimation of short-term reproductibility

Enrollment: 122
Study Start Date: January 2002
Estimated Study Completion Date: September 2006
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Adult non smokers, without any disease interfering with pulmonary function
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00213850


Locations
France
Service de Physiologie Clinique et des Explorations Fonctionnelles, Hôpital Civil
Strasbourg, France, 67091
Sponsors and Collaborators
University Hospital, Strasbourg, France
Investigators
Principal Investigator: Monique OSWALD-MAMMOSSER, MD Service de Physiologie Clinique et des Explorations Fonctionnelles, Hôpitaux Universitaires de Strasbourg
  More Information

ClinicalTrials.gov Identifier: NCT00213850     History of Changes
Other Study ID Numbers: 2667
First Submitted: September 13, 2005
First Posted: September 21, 2005
Last Update Posted: November 29, 2007
Last Verified: November 2007

Keywords provided by University Hospital, Strasbourg, France:
Interrupter technique
Respiratory resistance
Normal adults