Intrathecal Chloroprocaine for Lower Limb Arthroplasty

Hôpital de la Croix-Rousse

Status: Completed

Conditions: Lower Limb Arthroplasty Under Chloroprocaine Spinal Anesthesia

Treatments: Drug: Chloroprocaine Injection

Study type: Observational

Funder types: Other

Identifiers

NCT05365074

CSE-HCL 22_729

Details and patient eligibility

About

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

Full 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.

Enrollment: 65 patients

Sex

Volunteers: No Healthy Volunteers

Inclusion criteria

• adult patients
• with spinal anesthesia using 50 mg of chloroprocaine
• operated for total knee, unicompartment knee or anterior access hip arthroplasty
• in the period of years 2020 - 2021

Exclusion criteria

• expressed disagreement to to participate after receiving information notice

Trial design

65 participants in 1 patient group

chloroprocaine anesthesia for arthroplasty

Description:

patients having predicted uncomplicated surgery for total or unicompartment knee arthroplasty of anterior access total hip arthroplasty, operated under spinal anesthesia with 50 mg of chloroprocaine

Treatment:

Drug: Chloroprocaine Injection