The Effect of Pericapsular Nerve Group Block With Different Local Anesthetic Volumes

ConditionsPericapsuler Nerve Group Block Postoperative Pain

Trial statusNot yet recruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age18-65

SponsorSelcuk University

About this trial

Early postoperative pain following shoulder surgery is a significant clinical problem for both patients and orthopedic surgeons. Effective pain control is crucial for improving postoperative comfort and optimizing rehabilitation. Pericapsular nerve group block (PENG) is a regional anesthesia method that has recently gained attention due to its lack of motor block and absence of pulmonary complications. The aim of this study is to evaluate the effect of PENG block, applied at two different volumes, on postoperative pain and opioid consumption in patients undergoing arthroscopic shoulder surgery.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

elective arthroscopic shoulder surgery planned

ASA I-III physical status

Disqualifiers

coagulopathy,

neuropathy,

anticoagulant use

history of chronic pain,

Trial design

Design model

Parallel

Treatments tested in this trial

pericapsular nerve group (PENG) block
Procedure/Surgery
During PENG block application; the patient's arm was rotated externally and abducted at 45 degrees. A longitudinal linear ultrasound probe was placed between the coracoid and humeral head. After identifying the humeral head, the tendon of the subscapular muscle, and the deltoid muscle above it, a 50 mm needle was inserted using the "in-plane" technique. After the needle tip was placed above the bone below the subscapularis tendon, a local anesthetic solution was injected.

Treatment groups

60 Participants

are divided into 2 treatment groups

Group A: Group I; PENG block, 20 mL 0.5% bupivacaineActive comparator 1 intervention

Group B: Group II; PENG block, 40ml 0.25% bupivacaineActive comparator 1 intervention

Trial outcomes

Primary outcomes

postoperative pain and opiod consumption

Time frame

postoperative 24 hours

Locations

This trial has no locations.

Sponsors and contacts

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

Selcuk University

Lead sponsor

Source ClinicalTrials.gov

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