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RecruitingNCT04434586

Contribution of Optical Coherence Tomography in the Endovascular Treatment of Femoral Occlusions

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
166 (estimated)
Sponsor
University Hospital, Lille · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a common care study. A study for evaluating the quality of balloon inflation and stent application will be performed in 2D angiography alone in the control group and then by 2D and OCT angiography for the experimental group. The benefit could be an improvement in the results of revascularization of femoropopliteal lesions thanks to OCT which allows a 3D visualization of the arterial lumen.

Conditions

Interventions

TypeNameDescription
DEVICEfemoropopliteal revascularization for TASC C or TASC D lesionFemoropopliteal revascularization: ATL or ATL/stenting for TASC C/D lesions. Control group: only angiography 2D final control. Experimental group: angiography + OCT control

Timeline

Start date
2020-06-16
Primary completion
2026-06-01
Completion
2026-06-01
First posted
2020-06-17
Last updated
2025-12-23

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT04434586. Inclusion in this directory is not an endorsement.

Contribution of Optical Coherence Tomography in the Endovascular Treatment of Femoral Occlusions (NCT04434586) · Clinical Trials Directory