Clinical Trials in France / NCT07629843
Recruiting
Observational
Patient Satisfaction, Safety, and Efficacy of Endovenous Laser Treatment for Saphenous Veins and Varicose Veins
NCT07629843 · tracked via the Priya Life Science France tracker
Condition(s) studied
Saphenous Vein Injury
Investigational drug(s) / intervention(s)
Endovenous laser ablation of the primary or recurrent saphenous vein
Endovenous laser ablation of the primary or recurrent saphenous vein: Treatment of saphenous veins and varicose veins performed outside the operating room strictly under local anesthesia with a 1940 nm laser.
Study summary
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
Inclusion Criteria:
* 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.
* Patient has been informed and has verbally indicated their non-opposition to participating in the research.
Exclusion Criteria:
* 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.
* Patients currently participating or having participated in research within the previous 3 months.
* Persons covered by articles L1121-5 to L1121-8 of the French Public Health Code (corresponds to all protected persons: pregnant women, women in labor, breastfeeding mothers, persons deprived of liberty by judicial or administrative decision, persons subject to a legal protection measure).
Primary outcome measure(s)
- Venous Treatment Satisfaction Questionnaire early score — 12 days
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).
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Institut de Pathologie Vasculaire - Hôpital Privé Geoffroy Saint-Hilaire | Paris | France | Recruiting |
| Clinique de la Muette | Paris | France | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07629843 on ClinicalTrials.gov ↗ ← All trials in France