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Clinical Trial Summary

Study and evaluate the effectiveness of virtual reality in pain management.


Clinical Trial Description

Study and evaluate the effectiveness of virtual reality in pain management.This is an open prospective observational study carried out at Urgences Fattouma Bourgiba Monastir. For all patients included, a data collection form must be completed, mentioning age, sex, medical and surgical history, and the type of procedure planned. - If initial VAS >5 and intolerable: patients will immediately use painkillers and will be excluded from the study. - If initial VAS <=5 or > 5 but tolerable: Only VR glasses are used as an analgesic. If during the procedure the patient describes intolerable pain: the VAS will be noted, and the patient will use a rescue analgesic (intranasal ketamine or other at the discretion of the attending physician). The VR device consists of a pair of VR glasses with a video previously chosen and installed. Patient preparation must be done before initiating the protocol. The first step is to choose patient candidates for VR who are understanding and interested. Guardian approval is required; then it is necessary to explain the principle, the stages and the benefits of the care. The intensity of pain is calculated according to the visual analog scale before, during the procedure and 30 minutes after as well as the max VAS during the procedure, the 'Children Fear Scale', the satisfaction score and any adverse effects are noted. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06425835
Study type Observational [Patient Registry]
Source University of Monastir
Contact NOUIRA Semir, PR
Phone 73106000
Email semir.nouira@rns.tn
Status Not yet recruiting
Phase
Start date August 15, 2024
Completion date December 15, 2026

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