Comparison of IPACK and Adductor Canal Block Combination Versus Epidural Analgesia for Total Knee Arthroplasty

Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization

Status: Completed

Conditions: Knee Injuries

Treatments: Procedure: ipack+adduktor kanal

Study type: Observational

Funder types: Other

Identifiers

NCT05751109

681423

Details and patient eligibility

About

To compare the efficacy and complications of IPACK and adductor canal block combination and epidural block in patients who will be operated for knee arthroscopy under spinal anesthesia.

Full description

Between 15.08.2022 and 15.04.2023, the patients who will be operated on for knee surgery under spinal anesthesia, older than 18 years of age were included in the study. Demographic characteristics of the patients, comorbidities, ASA scores, mobilization time, amount of postoperative analgesic use, and postoperative pain scores of the 1. 8. 24. hours will be observed. The vas score at the 3rd month was learned over the phone.

Enrollment: 80 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Those who consented to participate in the study
• Patients over the age of 18 who will be operated on due to knee pathology
• Patients to be operated under spinal anesthesia
• Disease that will limit cooperation

Exclusion criteria

• Patients under the age of 18
• Patients to be operated under general anesthesia
• Disease that will cause limited cooperation

Trial design

80 participants in 2 patient groups

ipack+adductor canal block

Description:

The 40 patients received ACB + IPACK (Group 1, n = 40),. All patients were evaluated with VAS score for pain recorded at 1h, 8 h, postoperative day (POD) 1 and 3. month after the surgery. The secondary outcome measures assessed were movement time and discharge time.

Treatment:

Procedure: ipack+adduktor kanal

epidural analgesia

Description:

The 40 patients received combine spinal epidural (Group 2, n = 40),. All patients were evaluated with VAS score for pain recorded at 1h, 8 h, postoperative day (POD) 1 and 3. month after the surgery. The secondary outcome measures assessed were movement time and discharge time.

Treatment:

Procedure: ipack+adduktor kanal