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NCT00469313 Clinical Trial

Efficacy of Inspiratory Muscle Training on Inspiratory Capacity in Patients With COPD

COPD Clinical Trial

Official title:
Efficacy of Inspiratory Muscle Training on Inspiratory Capacity in Patients

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT00469313
Other study ID # L1234
Secondary ID
Status Enrolling by invitation
Phase N/A
First received May 2, 2007
Last updated May 21, 2008
Start date May 2007

Study information
Verified date May 2008
Source Hospital Hietzing
Contact n/a
Is FDA regulated No
Health authority Austria: Federal Institute for Drugs and Medical Devices
Study type Observational

Clinical Trial Summary

Hypothesis:benefits of inspiratory muscle strenght training with Respifit S decreases symptoms, disability or handicap of patients affected by COPD. The inspiratory fraction (inspiratory capacity IC/ total lung capacity TLC)may be functionally more representative than other traditional indices.

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 40 Years to 75 Years
Eligibility Inclusion Criteria:

- COPD GOLD II-III (FEV1<80 and >30%)

Exclusion Criteria:

- Pregnancy

- Lung cancer

- Diabetes mellitus

- Primary exacerbation of COPD

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Austria Hospital Hietzing Vienna

Sponsors (1)
Lead Sponsor Collaborator
Hospital Hietzing

Country where clinical trial is conducted

Austria, 

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