Minimally Invasive Superficial Venous Insufficiency Surgery and Digital Sedation
Recruiting
N/A
Interventional Study
Superficial Venous Insufficiency
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 400 (estimated)
- Sponsor
- GCS Ramsay Santé pour l'Enseignement et la Recherche · Other
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About This Trial
Virtual reality has been shown to reduce the pain experienced during medical procedures. The aim of this study is to determine to what extent the use of this technique could make it possible to defer the administration of neuroleptanalgesia during the endovenous thermal treatment of superficial varicose veins in addition to local anaesthesia by tumescence.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patient aged 18 or over, who has read and signed the consent form for participation in the study after a reflection period (approximately 1 hour).
* Outpatients with superficial venous insufficiency for which a surgical indication has been given
* Patient requiring sedation as…
Contacts