Patient Satisfaction, Safety, and Efficacy of Endovenous Laser Treatment for Saphenous Veins and Varicose Veins

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorGCS Ramsay Santé pour l'Enseignement et la Recherche

About this trial

The purpose of this study is to evaluate the post-operative patient satisfaction on the treatment of saphenous veins and varicose veins outside the operating theater under strict local anesthesia with a 1940 nm laser via the Venous Treatment Satisfaction Questionnaire early.

Eligibility criteria

Qualifiers

Age ≥ 18 years.

Endovenous Laser Ablation of a common or recurrent saphenous vein as part of routine care.

Clinical, Etiology, Anatomy, Pathophysiology, classification clinical stage.

Ability to understand the study objectives and complete questionnaires in French.

Disqualifiers

Endovenous Laser Ablation not feasible for technical reasons, particularly if the vein is too "bent" or there are endoluminal obstacles.

Episode of deep vein thrombosis less than 3 months ago or of superficial vein thrombosis less than 6 weeks ago.

Active cancer.

Geographical distance incompatible with study follow-up, according to the investigator's judgment.

Trial design

Treatments tested in this trial

  • Endovenous laser ablation of the primary or recurrent saphenous vein

Treatment groups

155 Participants
are divided into 1 treatment group

Sponsors and collaborators