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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02555202
Other study ID # LCADL (RB 15.037)
Secondary ID
Status Completed
Phase N/A
First received September 16, 2015
Last updated March 30, 2017
Start date October 15, 2015
Est. completion date September 30, 2016

Study information

Verified date September 2016
Source University Hospital, Brest
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The main objective of this study is to develop and to validate a French version of the London Chest Activity of Daily Living (LCADL) and the Dyspnea 12 and to determine the reliability of this version for the evaluation of the dyspnea in the Activity of Daily Living in COPD patients (stages severe and very severe).


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date September 30, 2016
Est. primary completion date September 30, 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- COPD with FEV1< 50% of predictive value

Exclusion Criteria:

- FEV1> 50% of predictive value

- Patients with an exacerbation of COPD in the previous 30 days the inclusion

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Brest University hospital Morlaix

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Brest

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary the Saint-Georges questionnaire, item Activity by comparison with item activities of the Saint-Georges questionnaire for the LCADL 15 days
Primary MMRC Dyspnea scale by comparison with MMRC dyspnea scale for the dyspnea 12 15 days
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