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

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01632033
First Posted: June 29, 2012
Last Update Posted: July 17, 2015
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 (Responsible Party):
University Hospital, Angers
  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 ]
    Predetermined scored . Scoring is optional and compared to scoring of the WIQ


Enrollment: 150
Study Start Date: July 2012
Study Completion Date: July 2014
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

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:   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
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): NCT01632033


Locations
France
University Hospital
Angers, France
Sponsors and Collaborators
University Hospital, Angers
Investigators
Study Chair: Denise JOLIVOT, MD University Hospital, Angers
  More Information

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
First Submitted: June 28, 2012
First Posted: June 29, 2012
Last Update Posted: July 17, 2015
Last Verified: July 2015

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