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Completed

NCT Number: NCT03356379

Popliteal Artery Entrapment Syndrome & TRanscutaneoUS Oxymetry

Aim of the study is to test the feasibility of transcutaneous oxygen pressure (TcPO2) recording in the diagnosis of popliteal entrapment syndrome (PES) in 30 patients with suspected PES and 30 asymptomatic control heathy subjects

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Key information

About this study

Patients suspected of PES and healthy cpontrols after detailled explanation of the protocol will have a recording of tcpO2 on both calves and will perform a series of elevation on foot in the standing position.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age over 18 years
  • Insurance company alffiliation Symptoms consistent with PES (patients) or absence of symptoms (controls)

Exclusion criteria

  • Refuse to participate Exclusion period from another protocole

Treatment and study plan

Transcutaneous oximetry

Diagnostic Test

Measurement of TcpO2 on calves and chests. Calculation of the DROP index (decrease from rest of oxygen pressure)on both calves

Primary outcomes

  1. Presence of a significant DROP decrease

    Time frame: 1 hour

    Comparison of DROP value between PES patients and controls

Sponsors and collaborators

Lead sponsor

University Hospital, Angers

Other Gov

Registry information

Official study title

Application de l'oxymétrie Dynamique Pour le Diagnostic Des pièges artériels poplités

Acronym: PETRUS

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Nov 29, 2017
Registry last updated
Dec 2, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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