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

NCT06790732 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2025-01-24

No results posted yet for this study

Summary

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.

Conditions

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

Interventions

DRUG

Saline

Patients received sham PENG block (just 1mL saline).

DRUG

Bupivacaine + Dexamethasone

Patients received real PENG block (15 mL of bupivacaine 0.25% +0.2mg/mL dexamethasone).

Sponsors & Collaborators

  • Tanta University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
21 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-05-01
Primary Completion
2024-05-01
Completion
2024-05-01

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06790732 on ClinicalTrials.gov