Evaluation of the Effectiveness of iPACK and Adductor Canal Blocks on Patients Undergoing Arthroscopic Knee Surgery
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-50
SponsorSakarya University
About this trial
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.
Eligibility criteria
Qualifiers
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
Disqualifiers
Coagulopathy
ASA IV-V patients
Uncooperable patients
Patients who refuses to participate in study
Trial design
Treatments tested in this trial
- IPACK and adductor canal block with Bupivacaine 0.25%
- Spinal Anesthesia with Bupivacaine
Treatment groups
64 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov