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NCT03357185: Eversion

Prospective Evaluation of Femoral Tripod Eversion Technique

Completed Last updated 29 July 2019
What this trial tests

trial testing Femoral eversion in Atheromatous in 37 participants. Completed in 30 September 2017.

Timeline
1 June 2014
Primary endpoint
30 April 2016
30 September 2017

Quick facts

Lead sponsorHôpital NOVO
StatusCompleted
Study typeOBSERVATIONAL
Enrollment37
Start date1 June 2014
Primary completion30 April 2016
Estimated completion30 September 2017

Drugs / interventions tested

Conditions studied

Sponsor

Hôpital NOVO — full company profile →

Who can join

18 and older, any sex, with Atheromatous. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Endarteriectomy is considered as the first line treatment of femoral bifurcation atheromatous lesions. Eversion technique, similar to that used for carotid bifurcation, is safe and possible for the majority of the femoral tripod lesions. The major advantage of the eversion technique is the absence of prosthetic material to be performed. However, its use has been scarcely evaluated in the literature to date. This work aims at evaluating the long term safety and the efficacy of eversion femoral technique. Surgical technique was thoroughly described and participants were followed up for two years by serial clinical and doppler US examination.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Atheromatous

Currently open trials in the same condition.

Other Hôpital NOVO trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03357185.

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