Viewing Study NCT06436118



Ignite Creation Date: 2024-06-16 @ 11:48 AM
Last Modification Date: 2024-10-26 @ 3:30 PM
Study NCT ID: NCT06436118
Status: COMPLETED
Last Update Posted: 2024-05-30
First Post: 2022-08-29

Brief Title: Evaluation of the Use of the RELAX Glasses on the Anxiety of Patients Undergoing Emergency Hand Surgery Under Locoregional Anesthesia
Sponsor: Centre Hospitalier de Valenciennes
Organization: Centre Hospitalier de Valenciennes

Study Overview

Official Title: Evaluation of the Use of the RELAX Glasses on the Anxiety of Patients Undergoing Emergency Hand Surgery Under Locoregional Anesthesia Compared to Those Who do Not Use the Glasses
Status: COMPLETED
Status Verified Date: 2024-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: RELAX
Brief Summary: More than 90 of hand surgery is performed under local anesthesia and can be a source of anxiety especially in an emergency context The management of this intraoperative anxiety is essential for the comfort The use of a virtual reality headset has shown its effectiveness in reducing anxiety in dental surgery or hand surgery under local anesthesia with the WALANT technique On the other hand virtual reality and the use of 3D can cause discomfort and side effects such as nausea and dizziness It is known that audiovisual distraction also effectively reduces pain and anxiety in patients with fewer side effects

The investigators have therefore chosen to use the RELAX glasses There are no publications examining the effectiveness of positive distraction as a non-pharmacological agent to improve the patient experience during emergency management in the operating room in the context of hand surgery under locoregional anesthesia The investigatos would like to study its action on the anxiety pain and global satisfaction
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None