ClinicalTrials.Veeva

Menu

Comparison of Interscalene and Pericapsular Nerve Group (PENG) Block in Shoulder Surgery

K

Kocaeli Derince Education and Research Hospital

Status

Unknown

Conditions

Visual Analogue Score

Treatments

Procedure: PENG Block

Study type

Interventional

Funder types

Other

Identifiers

NCT04718090
MYaziciKara-1

Details and patient eligibility

About

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.

Enrollment

34 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

34 participants in 2 patient groups

interscalene block
Active Comparator group
Treatment:
Procedure: PENG Block
PENG block
Active Comparator group
Treatment:
Procedure: PENG Block

Trial contacts and locations

0

Loading...

Central trial contact

İlke Kupeli, M.D.; Merve Yazici Kara, M.D.

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems