NCT05365074

Intrathecal Chloroprocaine for Lower Limb Arthroplasty

Perioperative Outcomes in Patients Received Spinal Chloroprocaine for Hip or Knee Arthroplasty

• Status: Completed
• Phase: —
• Study type: Observational
• Enrollment: 65 (actual)
• Sponsor: Hôpital de la Croix-Rousse · Academic / Other
• Sex: —
• Age: —
• Healthy volunteers: —

Summary

This study evaluates the perioperative course in adult patients undergoing total or partial knee arthroplasty, or total hip arthroplasty under chloroprocaine spinal anesthesia.

Detailed description

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.

Conditions

• Lower Limb Arthroplasty Under Chloroprocaine Spinal Anesthesia

Interventions

Type	Name	Description
DRUG	Chloroprocaine Injection	Spinal anesthesia with 50 mg of 1% Chloroprocaine

Timeline

• Start date: 2020-01-01
• Primary completion: 2021-12-31
• Completion: 2022-03-02
• First posted: 2022-05-09
• Last updated: 2022-05-09

Locations

1 site across 1 country: France