Lower Limb Arthroplasty Under Chloroprocaine Spinal Anesthesia Clinical Trial
Official title:
Perioperative Outcomes in Patients Received Spinal Chloroprocaine for Hip or Knee Arthroplasty
This study evaluates the perioperative course in adult patients undergoing total or partial knee arthroplasty, or total hip arthroplasty under chloroprocaine spinal anesthesia.
This study evaluates the failure rate of spinal anesthesia, the duration of surgical anesthesia, the needs for complementary intraoperative analgesia, the time for recovery, the incidence of urinary retention, postoperative nausea and vomiting, and length of stay in the recovery room in patients operated for knee or hip arthroplasty under spinal anesthesia with chloroprocaine 50 mg. ;