Audiovisual Distraction for Patients Undergoing Total Knee or Hip Replacement Surgery

Completed · Not applicable

Conditions studied: Anesthesia

In brief

The primary purpose of this study is to investigate whether audiovisual distraction can lead to a reduction in standard of care administered intraoperative propofol consumption compared to those who receive propofol sedation alone in adults having total hip or knee replacement surgery under spinal anesthesia.

Key facts

Study ID

NCT03191838

Run by

University of Utah

People needed

50

Starts

2017-11-01

Expected to finish

2020-06-01

Last updated by the study team

2020-08-11

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adults >18 years of age having a
• Primary total hip or knee arthroplasty
• Surgery under a spinal anesthetic

You may not qualify if…

• ASA status >3
• parturients
• documented hearing or vision loss
• chronic opioid use (>30mg PO MEQ daily for >1 month)
• diagnosis of OSA, contraindications to spinal (coagulopathy, infection, spinal hardware)
• non-English speaking
• current history of substance abuse
• schizophrenia
• generalized anxiety disorder
• Alzheimer's disease
• other dementia

Where it is running

• University of Utah — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

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