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

Knee Injuries Clinical Trial

Official title:

Comparison of Infiltration Between the Popliteal Artery and the Capsule of the Knee (IPACK) Block and Adductor Canal Block Combination Versus Epidural Analgesia for Total Knee Arthroplasty

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05751109
• Other study ID #: 681423
• Status: Completed
• Start date: August 1, 2022
• Est. completion date: October 1, 2023

Study information

• Verified date: January 2024
• Source: Prof. Dr. Cemil Tascioglu Education and Research Hospital Organization
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: October 1, 2023
• Est. primary completion date: August 16, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

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

Related Conditions & MeSH terms

• Knee Injuries

Intervention

Procedure:
• ipack+adduktor kanal
nerve block

Locations

Country	Name	City	State
Turkey	Onur Karaoglu	Istanbul	Kagithane
Turkey	Rasim Onur Karaoglu	Istanbul	Kagithane

Sponsors (1)

Lead Sponsor	Collaborator
Prof. Dr. Cemil Tascioglu Education and Research Hospital Organization

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Visual Analogue Scale (VAS) evaluation for postoperative pain	The Visual Analogue Scale (VAS) measures pain intensity. The VAS consists of a 10cm line, with two end points representing 0 ('no pain') and 10 ('pain as bad as it could possibly be').	8. Hour
Secondary	Visual Analogue Scale (VAS) evaluation for postoperative pain	The Visual Analogue Scale (VAS) measures pain intensity. The VAS consists of a 10cm line, with two end points representing 0 ('no pain') and 10 ('pain as bad as it could possibly be').	1. Hour
Secondary	Visual Analogue Scale (VAS) evaluation for postoperative pain	The Visual Analogue Scale (VAS) measures pain intensity. The VAS consists of a 10cm line, with two end points representing 0 ('no pain') and 10 ('pain as bad as it could possibly be').	24. Hour