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.
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.
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.
The study population will be composed of adult patients receiving routine care for Endovenous Laser Ablation of primary or recurrent saphenous vein (great saphenous vein, small saphenous vein or anterior saphenous vein) outside the operating theater under strict local anesthesia.
Cohort
Prospective
Endovenous laser ablation of the primary or recurrent saphenous vein
Procedure/SurgeryTreatment of saphenous veins and varicose veins performed outside the operating room strictly under local anesthesia with a 1940 nm laser.
Venous Treatment Satisfaction Questionnaire early score
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. Scale from 0 to 6 (a high score indicates a positive result).
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GCS Ramsay Santé pour l'Enseignement et la Recherche
Lead sponsor
Euraxi Pharma
Collaborator
This trial is not recruiting at the moment. You can still explore other options: