Skip to main content
Clinical Trials/NCT04718090
NCT04718090
Unknown
Not Applicable

Comparison of Postoperative Analgesic Consumption and Pain in Shoulder Surgery Patients Undergoing Interscalene and Pericapsular Nerve Group (PENG) Blocks

Kocaeli Derince Education and Research Hospital0 sites34 target enrollmentFebruary 1, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Visual Analogue Score
Sponsor
Kocaeli Derince Education and Research Hospital
Enrollment
34
Primary Endpoint
Visual Analogue Scale
Last Updated
5 years ago

Overview

Brief Summary

Early postoperative pain after shoulder surgery is a major concern and distress for patients and orthopedic surgeons. Adequate pain control; It is vital for all aspects of patient recovery, including mental state, nutrition, cost of care period, rehabilitation, patient satisfaction, and overall post-surgery outcomes.Single analgesic regimens are not always effective in controlling moderate to severe postoperative pain.Therefore, multimodal pain management is preferred and is currently recommended for early postoperative pain control.Regional anesthesia is preferred in shoulder surgery as an effective way to provide anesthesia and postoperative analgesia.To ensure adequate postoperative pain control, nerve supply to the synovium, capsule, joint surfaces, ligaments, periosteum and shoulder muscles must be blocked.Interscalene blocks are well studied and established means of providing analgesia following shoulder surgery and are considered the gold standard mode of regional anesthesia.Pericapsular nerve group block is a new block that provides a pericapsular distribution with local anesthetic infiltration around the glenohumeral joint and provides analgesia without motor blockage by reaching the sensory nerve branches of the glenohumeral joint.The aim of this study was to compare the results between interscalene block and pericapsular nerve group block in patients undergoing shoulder surgery.

Registry
clinicaltrials.gov
Start Date
February 1, 2021
End Date
July 31, 2021
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Kocaeli Derince Education and Research Hospital
Responsible Party
Principal Investigator
Principal Investigator

Merve Yazici Kara

M.D.

Kocaeli Derince Education and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • 18 years and over
  • American Society of Anesthesiologists (ASA) 1 and 2
  • shoulder surgery

Exclusion Criteria

  • under 18 years old
  • American Society of Anesthesiologists (ASA) 3 and above
  • who are allergic to local anesthetics
  • patients with infection at the injection site
  • pregnant women

Outcomes

Primary Outcomes

Visual Analogue Scale

Time Frame: 5 months

Visual Analogue Scale

Similar Trials