Interscalene Block Versus Infraspinatus-Teres Minor Interfascial Plane Block for Shoulder Arthroscopy

ConditionsPostoperative Pain Shoulder Arthroscopic Surgeries Diaphragmatic Dysfunction

Trial statusNot yet recruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age18-65

SponsorTC Erciyes University

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

This trial does not accept healthy volunteers

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

Design model

Parallel

Treatments tested in this trial

Ultrasound-Guided Interscalene Block
Procedure/Surgery
Ultrasound-guided interscalene brachial plexus block is performed before induction of anesthesia for postoperative analgesia in patients undergoing shoulder arthroscopy. The block is administered using ultrasound guidance according to institutional practice.
Ultrasound-Guided Infraspinatus-Teres Minor Interfascial Plane Block
Procedure/Surgery
Ultrasound-guided infraspinatus-teres minor interfascial plane block is performed before induction of anesthesia for postoperative analgesia in patients undergoing shoulder arthroscopy. The block is administered using ultrasound guidance according to institutional practice.

Treatment groups

120 Participants

are divided into 3 treatment groups

Group A: Interscalene Block GroupExperimental treatment 1 intervention

Group B: Infraspinatus-Teres Minor Interfascial Plane Block GroupExperimental treatment 1 intervention

Group C: Control GroupNo intervention 0 interventions

Trial outcomes

Primary outcomes

Postoperative Pain Intensity

Postoperative pain intensity assessed using the Visual Analog Scale (VAS) , ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. higher scores indicate greater pain intensity. compared between study groups.

Time frame

0, 2,4, 6, 12, and 24 hours after surgery

Diaphragmatic Excursion

Comparison of postoperative diaphragmatic excursion measured by ultrasonography between study groups.

Time frame

24 hours after surgery

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

TC Erciyes University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: