Functional Evaluation With Questionnaire in Patients Investigated for Suspected Peripheral Artery Disease (WELCH-bis)

This study is currently recruiting participants.
Verified July 2012 by University Hospital, Angers
Sponsor:
Information provided by (Responsible Party):
University Hospital, Angers
ClinicalTrials.gov Identifier:
NCT01632033
First received: June 28, 2012
Last updated: July 17, 2012
Last verified: July 2012
  Purpose

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.


Condition
Peripheral Artery Disease

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
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

Resource links provided by NLM:


Further study details as provided by University Hospital, Angers:

Primary Outcome Measures:
  • Scoring of the WELCH. Percent scored questionnaires [ Time Frame: 1 day ] [ Designated as safety issue: No ]
    Predetermined scored . Scoring is optional and compared to scoring of the WIQ


Estimated Enrollment: 700
Study Start Date: July 2012
Estimated Study Completion Date: July 2014
Estimated Primary Completion Date: July 2014 (Final data collection date for primary outcome measure)
Groups/Cohorts
Investigation for lower limb arteries
Patients referred for investigation of assumed peripheral artery disease (PAD)

Detailed Description:

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

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Patients referred for arterial leower limb investigations

Criteria

Inclusion Criteria:

  • Sigjned consent for the data treatment as a database

Exclusion Criteria:

  • Non french native language age < 18 years old
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01632033

Contacts
Contact: Pierre Abraham, MD; PhD +33 241353637 piabraham@chu-angers.fr
Contact: Denise JOLIVOT, MD dejolivot@chu-angers.fr

Locations
France
University Hospital Recruiting
Angers, France
Contact: P Abraham       piabraham@chu-angers.fr   
Principal Investigator: P Abraham, MD, PhD         
Sponsors and Collaborators
University Hospital, Angers
Investigators
Study Chair: Denise JOLIVOT, MD University Hospital, Angers
  More Information

No publications provided by University Hospital, Angers

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: University Hospital, Angers
ClinicalTrials.gov Identifier: NCT01632033     History of Changes
Other Study ID Numbers: PL 2012/14
Study First Received: June 28, 2012
Last Updated: July 17, 2012
Health Authority: France: Ministry of Health

Keywords provided by University Hospital, Angers:
Peripheral artery disease
claudication
walking
questionnaire

Additional relevant MeSH terms:
Peripheral Arterial Disease
Atherosclerosis
Arteriosclerosis
Arterial Occlusive Diseases
Vascular Diseases
Cardiovascular Diseases
Peripheral Vascular Diseases

ClinicalTrials.gov processed this record on April 17, 2014