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NCT05796076

Virtual Reality to Reduce Anxiety and Pain During Suturing Procedure

Completed NA Last updated 16 April 2024
What this trial tests

NA trial testing Virtual reality in Suture in 80 participants. Completed in 9 August 2023.

Timeline
3 February 2023
Primary endpoint
9 August 2023
9 August 2023

Quick facts

Lead sponsorTuen Mun Hospital
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposehealth services research
Enrollment80
Start date3 February 2023
Primary completion9 August 2023
Estimated completion9 August 2023
Sites1 location across Hong Kong

Drugs / interventions tested

Conditions studied

Sponsor

Tuen Mun Hospital

Who can join

Adults 18 to 65, any sex, with Suture. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Background: In emergency departments, suturing is a common procedure but often causes anxiety and pain. Virtual reality (VR) intervention has been reported as a relaxing measure. Objective: The study aims to examine the effects of VR intervention on anxiety, pain, physiological parameters, local anaesthesia requirements and satisfaction in Chinese adult patients undergoing wound closure in emergency departments in Hong Kong Hypothesis:VR can alleviate anxiety and pain experienced by Chinese adult patients undergoing wound-closure procedures, the intervention can decrease extra local anesthesia requirements and physiological parameters during the procedures, and the intervention can significantly increase satisfaction during wound-closure procedures.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of Virtual reality

Trials testing the same drug.

Other Tuen Mun Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05796076.

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