A Study to Evaluate Virtual Reality As Adjunct to Anesthesia During Orthopedic Surgery

NCT ID: NCT05112302

Last Updated: 2026-01-21

Study Results

Results pending

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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Recruitment Status

ENROLLING_BY_INVITATION

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-08-17

Study Completion Date

2026-12-31

Brief Summary

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The purpose of this study is to obtain feedback from patients and orthopedic surgeons who agree to use virtual reality (VR ) as an adjunct to standard of care in orthopedic cases under regional or central neuraxial nerve block. This will serve as a preliminary study for future trials to compare outcomes between VR and standard of care vs standard of care only.

Detailed Description

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Conditions

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Knee Arthropathy Hip Injuries

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Virtual reality

Virtual reality

Intervention Type OTHER

Use of virtual reality goggles during procedure

Interventions

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Virtual reality

Use of virtual reality goggles during procedure

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age ≥ 18 years old.
* 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

* Age \< 18 years old.
* 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).
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Mayo Clinic

OTHER

Sponsor Role lead

Responsible Party

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Klaus D. Torp

Principal Investigator

Responsibility Role 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

Site Status

Countries

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United States

Related Links

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Other Identifiers

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21-005305

Identifier Type: -

Identifier Source: org_study_id

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