Intraoperative management of critical arrhythmia.
Chang Hee Kwon, Seong-Hyop Kim
https://pubmed.ncbi.nlm.nih.gov/28367281/Actively Recruiting
Led by Belfast Health and Social Care Trust · Updated on 2025-05-08
40
Participants Needed
1
Research Sites
N/A
Total Duration
This research evaluates the use of virtual reality VR alongside spinal anaesthesia during total knee arthroplasty TKA. The study aims to determine if VR can reduce the need for deeper sedation while maintaining patient satisfaction and potentially lowering side effects commonly linked to sedation such as nausea, confusion, and breathing difficulties. It also explores the feasibility and outcomes of VR use in this surgical setting. Participants will all receive spinal anaesthesia. They are randomly assigned to one of two groups one group will use VR combined with light sedation, while the other group will receive standard care with deeper sedation but no VR. The study compares these approaches to assess if VR can help reduce sedation dosage and related side effects during TKA. During the study, patients will be monitored for sedation levels, recovery quality, and complications up to one week after surgery. Researchers will assess various outcomes including sedation amount, cognitive tests, mobilization time, pain management, anti-nausea medicine use, and hospital stay length. The primary outcome is to evaluate the feasibility of using VR during TKA with spinal anaesthesia, measured the day after surgery.
CONDITIONS
Can the Use of Virtual Reality Improve TKA Outcomes
N
Nicola Gallagher
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Belfast Health and Social Care Trust
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of surgery
Participants undergo total knee arthroplasty with spinal anaesthesia and limited propofol sedation, with or without virtual reality during surgery.
1 surgical visit
Duration - Up to 1 week post operation
Participants are observed and assessed for recovery quality, sedation effects, complications, and mobilisation following surgery.
Several visits including assessments at 1 hour, 4 hours, 24 hours, and 48 hours after surgery, plus monitoring up to 1 week
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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Lead Sponsor