Virtual reality during loco regional anesthesia for knee arthroplasty

Not Applicable

Recruiting

• Conditions: Orthopaedics; Anaesthesia

• Registration Number: PACTR202308639904589
• Lead Sponsor: Sahloul Teaching Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-08-07
• Last Update Posted: 4 March 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 66

Inclusion Criteria

•Age 18 years or more
•ASA I or II
•Acceptance to participate to the study

Exclusion Criteria

•Patients who had an intra operative incident (bleeding, bronchospasm, anaphylaxis)
•Patients who needed a conversion to general anesthesia
•Patients who required a transfer to intensive care unit
•Visual and auditory impairments
•History of epilepsy
•Cognitive disorders
•Contraindications to spinal anesthesia
•Ambulatory surgery
•Neuropsychiatric disorders
•Analgesics chronic use

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Patient satisfaction - likert scale

Secondary Outcome Measures

Name	Time	Method
post operative opioids requirements;Time to rescue analgesia;Post operative Pain intensity- Visual Analogue scale;Hemodynamic stability ;postoperative ambulation;Quality of rehabilitation- QoR40;Length of hospital stay