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CompletedNCT01632033WELCH-bisUpdated Jul 17, 2015

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

An observational study in Peripheral Artery Disease, sponsored by University Hospital, Angers. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2015-07-17.

Sponsored by University Hospital, Angers · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
150
Ages
18 Years and older
Sex
All
01

Study 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.

Read the detailed description

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

02

Conditions studied

  • Peripheral Artery Disease

Keywords

  • Peripheral artery disease
  • claudication
  • walking
  • questionnaire
03

In context

Peripheral Arterial Disease

1,573 studies on the registry are indexed under Peripheral Arterial Disease; 284 are open to participants now.

This study's enrollment of 150 is below the median of 190 across 427 observational studies indexed under Peripheral Arterial Disease.

Browse Peripheral Arterial Disease studies →

Lead sponsor

University Hospital, Angers is the lead sponsor of 477 studies on the registry; 119 are open to participants now.

Browse University Hospital, Angers studies →

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients referred for arterial leower limb investigations

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Sigjned consent for the data treatment as a database

Exclusion criteria

Exclusion Criteria:

  • Non french native language age \< 18 years old
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
150 participants (actual)

Groups and cohorts

  • Investigation for lower limb arteries

    Patients referred for investigation of assumed peripheral artery disease (PAD)

06

What researchers measure

Primary outcomes

  1. Scoring of the WELCH. Percent scored questionnaires

    Predetermined scored . Scoring is optional and compared to scoring of the WIQ

    Time frame: 1 day

07

Study locations

1 site
  • University Hospital
    Angers, France
08

References and documents

Publications

  • Ouedraogo N, Chanut M, Aubourg M, Le Hello C, Hidden V, Audat G, Harbonnier M, Abraham P. Development and evaluation of the Walking Estimated-Limitation Calculated by History questionnaire in patients with claudication. J Vasc Surg. 2013 Oct;58(4):981-8. doi: 10.1016/j.jvs.2013.03.039. Epub 2013 May 7. PubMed 23663870 ↗
09

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Jul 2012, a primary completion of Jul 2014 and a completion of Jul 2014. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 28, 2012
First posted
Jun 29, 2012
Start
Jul 2012
Primary completionActual
Jul 2014
CompletionActual
Jul 2014
Last update
Jul 17, 2015
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 17, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01632033
Lead sponsor
University Hospital, Angers
Responsible party
Sponsor
First posted
Jun 29, 2012
Start date
Jul 2012
Primary completion
Jul 2014
Completion
Jul 2014
Last update
Jul 17, 2015

Study contacts

Denise JOLIVOT, MD
study chair · University Hospital, Angers

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2015. You cannot join it, but the record below documents what was studied.

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Discussion

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