ClinicalTrials.Veeva

Menu

Preoperative Ultrasound-Guided Peri- Capsular Nerve Group Block on Postoperative Analgesia After Shoulder Arthroscopic Surgery

T

Tanta University

Status

Completed

Conditions

Shoulder Arthroscopic Surgery
Postoperative Analgesia
Preoperative
PeriCapsular Nerve Group Block
Ultrasound-Guided

Treatments

Drug: Bupivacaine + Dexamethasone
Drug: Saline

Study type

Interventional

Funder types

Other

Identifiers

NCT06790732
36264MS117/3/23

Details and patient eligibility

About

This study aimed to evaluate the analgesic efficacy of preoperative ultrasound-guided peri-capsular nerve group block (PENG) on postoperative analgesia after shoulder arthroscopic surgery.

Full description

Postoperative pain control after shoulder surgery is challenging, and poor pain management is invariably reflected in poor outcomes, with longer hospitalization and recovery time. The difficulty in reducing pain due to the complexity of shoulder innervation leads to conducting studies to explore selective axillary nerve blocks with a posterior approach or from the axillae.

The peri-capsular nerve group (PENG) block is a regional anesthetic technique. It can be effectively and safely applied under ultrasound guidance in shoulder surgery cases for postoperative analgesia. It targets only the sensory branches and not the posterior mechanoreceptors; there is a potential motor-sparing effect which is desirable for better physical therapy, and earlier discharge.

Enrollment

60 patients

Sex

All

Ages

21 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age from 21 to 65 years.
  • Both sexes.
  • American Society of Anesthesiologists (ASA) physical status I-III.
  • Scheduled for unilateral shoulder arthroscopic surgery.

Exclusion criteria

  • Patient refusal.
  • Known hypersensitivity to local anesthetics.
  • Body mass index> 35 kg /m2.
  • Uncooperative or psychiatric patients.
  • Infection at the injection site.
  • Coagulation disorder.
  • Major cardiac, renal, or hepatic diseases.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

Control Group
Sham Comparator group
Description:
Patients received sham PENG block (just 1mL saline).
Treatment:
Drug: Saline
PeriCapsular Nerve Group Block (PENG) Group
Experimental group
Description:
Patients received real PENG block (15 mL of bupivacaine 0.25% +0.2mg/mL dexamethasone).
Treatment:
Drug: Bupivacaine + Dexamethasone

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems