About this trial
This prospective randomized controlled study aims to compare the effects of interscalene block, infraspinatus-teres minor interfascial plane block, and a control group on postoperative analgesia and diaphragmatic function in patients undergoing shoulder arthroscopy. A total of 120 patients will be enrolled and allocated into three groups. Postoperative pain scores, opioid consumption, rescue analgesic requirements, and diaphragmatic function will be evaluated and compared among the groups. The study seeks to determine whether the infraspinatus-teres minor interfascial plane block can provide effective postoperative analgesia with less impact on diaphragmatic function compared with interscalene block.
Eligibility criteria
Qualifiers
Age between 18 and 65 years
ASA physical status I-II
Scheduled for elective shoulder arthroscopy
No known allergy to study medications
Disqualifiers
Refusal to participate
Uncontrolled hypertension
Chronic pain or ongoing analgesic treatment
Significant cardiac disease (coronary artery disease, arrhythmia, heart failure)
Trial design
Treatments tested in this trial
- Ultrasound-Guided Interscalene Block
- Ultrasound-Guided Infraspinatus-Teres Minor Interfascial Plane Block