Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
ID07092982

Comparison of Ultrasound-Guided Adductor Canal Block with iPACK Block versus Suprainguinal Fascia Iliaca Block on Postoperative Pain and Stress in Total Knee Arthroplasty Patients

Led by SB Istanbul Education and Research Hospital · Updated on 2026-04-06

52

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Patients undergoing total knee arthroplasty often face severe pain after surgery, which can delay recovery and lead to complications like infections and longer hospital stays. This research compares two regional anesthesia techniques used to control postoperative pain and reduce opioid use: the Suprainguinal Fascia Iliaca Block and the combination of Adductor Canal Block with iPACK Block. The study aims to evaluate how these methods affect postoperative pain, stress response, and motor function in these patients. The study involves two groups: one group receives the Suprainguinal Fascia Iliaca Block with 30 ml of 0.25% Bupivacaine at the end of surgery, and the other group receives a combination of Adductor Canal Block and iPACK Block, each with 15 ml of 0.25% Bupivacaine. Both procedures are guided by ultrasound. Researchers will compare opioid consumption, pain scores at rest and during movement, time until the first need for pain relief, muscle strength, nausea, recovery quality, and inflammatory markers within 24 hours after surgery. Participants will be monitored closely during the first 24 hours after surgery with assessments of pain, muscle strength, inflammation markers like IL-6 and CRP, and opioid usage. The study uses double-blind randomized methods to ensure unbiased results. Patient recovery quality and side effects such as nausea will also be tracked. The total participation involves the immediate postoperative period up to 24 hours, focusing on early pain control and stress response outcomes.

CONDITIONS

Brief Title

Comparison of Two Different Regional Anesthetic Methods in Total Knee Arthroplasty Patients

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients undergoing total knee arthroplasty
  • Patients aged 18 to 75 years
  • Patients with ASA physical status I, II, or III
Not Eligible

You will not qualify if you...

  • Coagulation disorders
  • Allergy to local anesthetics
  • Liver or kidney failure
  • Alcohol or drug addiction
  • Cognitive problems preventing pain assessment
  • Systemic or injection site infection
  • Use of analgesics for more than 3 months
  • Refusal to participate or give consent
  • Presence of hematoma, hernia, neoplasm, or similar at the block site
  • Existing neurological deficits
  • Contraindications to nerve block

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Up to 24 hours

Participants undergo total knee arthroplasty surgery and receive one of two regional anesthetic methods at the end of the operation to manage postoperative pain.

1 surgical procedure visit

Trial Site Locations

Total: 1 location

1

SB Istanbul Education and Research Hospital

Istanbul, Turkey (Türkiye)

Actively Recruiting

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Research Team

K

Kubilay Ekinci, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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