A Study to Evaluate Virtual Reality As Adjunct to Anesthesia During Orthopedic Surgery
NCT ID: NCT05112302
Last Updated: 2026-01-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ENROLLING_BY_INVITATION
50 participants
OBSERVATIONAL
2021-08-17
2026-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Virtual reality
Virtual reality
Use of virtual reality goggles during procedure
Interventions
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Virtual reality
Use of virtual reality goggles during procedure
Eligibility Criteria
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Inclusion Criteria
* Patients scheduled for orthopedic procedure under regional or central neuraxial nerve block (anterior primary hip arthroplasty or primary knee arthroplasty).
* Subject willing to participate and able to provide informed consent.
Exclusion Criteria
* History of motion sickness or blindness.
* Unable to consent due to cognitive difficulty.
* Current diagnosis of epilepsy, dementia, or other neurological disease that may prevent use of VR hardware and software.
Sensitivity to flashing light or motion.
* Recent stroke.
* Injury to the eyes, face, neck, or arms that prevents comfortable use of VR hardware or software, or safe use of the hardware (e.g., open wound, sores, or skin rash on face).
18 Years
ALL
No
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Klaus D. Torp
Principal Investigator
Principal Investigators
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Klaus Torp, MD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic in Florida
Jackson, Florida, United States
Countries
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Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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21-005305
Identifier Type: -
Identifier Source: org_study_id
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