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RECRUITING
NCT06336447
NA

VR and Cooled Genicular Nerve Radio Frequency Ablation for Chronic Knee Pain

Sponsor: Northwestern University

View on ClinicalTrials.gov

Summary

This study will examine the impact of virtual reality used in conjunction with sedation compared to sedation alone in patients undergoing watervcooled genicular nerve ablations for chronic knee pain. The goals of the study is to determine the relative efficacy of virtual reality as a distraction modality when used as an adjuvant to procedural sedation compared to sedation alone for procedure related pain. To assess procedural satisfaction, and 1-month pain and functional outcomes.To explore whether virtual reality and lower procedure-related pain scores affect 1-month outcomes. And finally to determine whether demographic and clinical characteristics are associated with outcome measures.

Official title: Can Virtual Reality Improve Patient Tolerance in Patients Undergoing Water Cooled Genicular Nerve Radio Frequency Ablation in Patients With Chronic Knee Pain? A Randomized Controlled Trial

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

62

Start Date

2024-01-12

Completion Date

2027-02-28

Last Updated

2024-03-28

Healthy Volunteers

No

Conditions

Interventions

OTHER

Experimental: Group #1: Virtual Reality Headset

Group 1 will be assigned to the Virtual Realtity Headset. Participants will wear the device for at least 10 minutes prior to the planned procedure. Subjects will receive standard procedure. The VR Headset will be removed 10 minutes after the planned procedure.

OTHER

Group 2 No Virtual Reality Headset

Group 2 will receive standard care without the use of the Virtuality Reality Heaset.

Locations (1)

Northwestern Medicine Pain Center

Chicago, Illinois, United States