Actively Recruiting
Evaluation of the Effectiveness of iPACK and Adductor Canal Blocks on Patients Undergoing Arthroscopic Knee Surgery
Led by Sakarya University · Updated on 2026-02-06
64
Participants Needed
1
Research Sites
39 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Arthroscopic knee surgery is one of the most commonly performed procedures in orthopedic surgery. More than 50% of patients experience moderate to severe pain after the operation. Inadequate postoperative pain control and poor recovery quality can negatively impact physiotherapy protocols, prolong hospital stays, and consequently lead to cognitive dysfunction, systemic infections, and increased healthcare costs. Therefore, reducing postoperative pain and improving recovery quality are of great importance. In our clinic, a variety of analgesic techniques are routinely employed as part of a multimodal analgesia approach for patients undergoing arthroscopic knee surgery. One of these techniques is the simultaneous application of the IPACK block and the adductor canal block. In this study, we aim to evaluate the effectiveness of these blocks on postoperative recovery quality in patients undergoing arthroscopic knee surgery.
CONDITIONS
Official Title
Evaluation of the Effectiveness of iPACK and Adductor Canal Blocks on Patients Undergoing Arthroscopic Knee Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged between 18 and 50 years
- Scheduled for arthroscopic knee surgery under spinal anesthesia due to knee pathology
- Patients classified as ASA physical status I-II-III according to the American Society of Anesthesiologists risk classification
You will not qualify if you...
- Coagulopathy
- ASA IV-V patients
- Uncooperable patients
- Patients who refuse to participate in the study
- Patients taking chronic pain treatments
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Sakarya University Training and Research Hospital
Sakarya, Turkey (Türkiye)
Actively Recruiting
Research Team
O
Oğuzhan Okumuş, M.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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