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Popliteal Artery Entrapment Syndrome & TRanscutaneoUS Oxymetry

Not Applicable
Completed
Conditions
Popliteal Entrapment Syndrome
Registration Number
NCT03356379
Lead Sponsor
University Hospital, Angers
Brief Summary

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

Detailed Description

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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Presence of a significant DROP decrease1 hour

Comparison of DROP value between PES patients and controls

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

CHU Angers

🇫🇷

Angers, France

CHU Angers
🇫🇷Angers, France

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