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Clinical Trial Summary

The aim of our study is to compare patients anxiety and pain during percutaneous vascular interventions with and without virtual reality autohypnosis.


Clinical Trial Description

The participants in the control group will be treated under local anesthesia, following the usual care protocols. The participants in the experimental group will be treated under the same conditions, except that they will experience virtual reality autohypnosis during the intervention. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04561596
Study type Interventional
Source University of Lausanne
Contact Salah Dine Qanadli, Prof. MD PhD
Phone +41213144560
Email [email protected]
Status Recruiting
Phase N/A
Start date September 23, 2020
Completion date December 31, 2021

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