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Clinical Trials/NCT03362710
NCT03362710
Completed
Not Applicable

Evaluation du Risque Vasculaire Par Mesures Non Invasives en Soins Primaires.

University Hospital, Angers1 site in 1 country225 target enrollmentApril 9, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Artery Disease, Peripheral
Sponsor
University Hospital, Angers
Enrollment
225
Locations
1
Primary Endpoint
Performance of non-invasive measurements
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Peripheral artery disease (PAD) affects mainly elderly patients. The ankle brachial index (ABI) and ultrasound imaging are the standard diagnostic tools in PAD diagnostic and severity estimation. Measurements are generally performed by a vascular physician. However, access to medical specialist is becoming increasingly difficult with long waiting times while the aging of the population increases, while most of these patients are seen by the general practitioner.

To date, there is a lot of data in the literature on the value of using various ambulatory devices in the diagnosis and severity estimation of PAD but studied one by one.

The investigators propose to compare the measurements made by a series of simple non-invasive ambulatory tools with the measurements performed by the vascular specialist. The investigators wish to demonstrate that a series of simple and economical tools, available to paramedical health professionals can diagnose PAD and evaluate ts severity the reducing the direct and indirect associated costs.

Detailed Description

Patients referred for an arterial vascular investigations of the lower limbs will be included. After signing the consent, all included patients will be assessed by the examination series, among which ABI measurement and an arterial Doppler ultrasound of the lower limbs +/- transcutaneous oxygen pressure recording in case of suspected critical limb ischemia. Following the visit patients will be classified as have or not PAD and in case of PAD classified for the severity of PAD on the basis of the investigation results. Blinded to the results of the vascular laboratory test, a technician will: Measure ABI with an automatic sphygmomanometer. Examination series: 1. Skin temperature on the back of the foot with infra-red thermometry 2. Toe saturometry 3. ABI with an automatic sphygmomanometry 4. Skin Recoloration time at the foot

Registry
clinicaltrials.gov
Start Date
April 9, 2018
End Date
March 30, 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
University Hospital, Angers
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients referred for arterial assessment of the lower limbs as part of a screening or follow-up of PAD
  • Patients without contraindications for all non-invasive measures
  • Age superior to 18 years
  • Affiliated patients of a social security scheme
  • Patients who have signed informed consent.

Exclusion Criteria

  • Patients protected by law
  • Patients unable to understand the objectives or instructions of the study
  • Patients in an exclusion period relative to another biomedical study.

Outcomes

Primary Outcomes

Performance of non-invasive measurements

Time Frame: 1 hour

Performance of the score will be studied with the receiver operating characteristic (ROC) approach and multivariate analysis using echo-doppler and transcutaneous oxymetry results as references for PAD severity classification standard

Study Sites (1)

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