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NCT01632033 Clinical Trial

Functional Evaluation With Questionnaire in Patients Investigated for Suspected Peripheral Artery Disease

Peripheral Artery Disease Clinical Trial

— WELCH-bis  

Official title:
Estimation de la capacité Fonctionnelle a la Marche Par Questionnaire Clinique Chez Des Patients adressés Pour Bilan artériel Des Membres inférieurs: Etude WELCH-bis

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01632033
Other study ID # PL 2012/14
Secondary ID
Status Completed
Phase N/A
First received June 28, 2012
Last updated July 16, 2015
Start date July 2012
Est. completion date July 2014

Study information
Verified date July 2015
Source University Hospital, Angers
Contact n/a
Is FDA regulated No
Health authority France: Ministry of Health
Study type Observational

Clinical Trial Summary

The purpose of this study is to test the routine faisibility of a questionnaire to estimate walking impairment(The WELCH questionnaire) in patients investigated for suspected PAD.

Description:

The WELCH and WIQ questionnaires are self completed by the patients and scored by the physician after self-completion.

Recruitment information / eligibility
Status Completed
Enrollment 150
Est. completion date July 2014
Est. primary completion date July 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Sigjned consent for the data treatment as a database

Exclusion Criteria:

- Non french native language age < 18 years old

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
France University Hospital Angers

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Angers

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Scoring of the WELCH. Percent scored questionnaires Predetermined scored . Scoring is optional and compared to scoring of the WIQ 1 day No
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