drugset / Trial / NCT05706844

Spinal Anaesthesia vs. General Anaesthesia for THA, TKA and UKA

NCT05706844

Phase 4 Completed 222 enrolled Anders Troelsen Vejle Hospital · collab
RandomizedParallel-groupSingle-blindTreatment

Summary

The goal of this randomized clinical trial is to investigate the postoperative recovery following hip and knee arthroplasty procedures depending on the use of either spinal anaesthesia (SA) or general anaesthesia (GA). The main questions are: * Are more patients able to be safely mobilized within 6 hours postoperatively when using GA compared to SA? * Does postoperative pain, nausea and vomiting, dizzyness, occurence of delirium and urinary retention differ between the anaesthetic methods? Participants, scheduled for total hip, total knee and unicomartmental knee arthroplasty, will be randomized to recieve spinal anaesthesia or general anaesthesia in relation to surgery. At 6 hours postoperatively a physiotherapist will conduct a 5-meter walking test to evaluate whether the participant can be safely mobilized.

Timeline

Start
2023-03-06
Primary completion
2025-04-06
Completion
2025-04-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Bupivacaine Other / unclassified 10 mg Intrathecal
Subject Propofol Small molecule 3 mg/kg Intravenous
Subject Propofol Small molecule 5 mg/kg Intravenous
Subject Remifentanil Small molecule 0.5 ug/kg Intravenous