Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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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