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

Sponsor
Selcuk University
Study ID
NCT07666737
Status
Not Yet Recruiting

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Conditions

  • Pericapsuler Nerve Group Block
  • Postoperative Pain

Eligibility Criteria

Sex
ALL
Age
18 Years - 65 Years
Healthy Volunteers
Not accepted

Interventions

  • pericapsular nerve group (PENG) block — PROCEDURE
    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.

Study Details

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.

Key Dates

First listed
Jun 24, 2026
Start date
Jul 1, 2026
Status verified
Jun 2026
Primary completion
Jan 1, 2027
Completion
Feb 1, 2027

Study Design

Enrollment
60 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE

Arms

  • Active Comparator: Group I; PENG block, 20 mL 0.5% bupivacaine
  • Active Comparator: Group II; PENG block, 40ml 0.25% bupivacaine

Primary Outcome Measure

postoperative pain and opiod consumption [ Time Frame: postoperative 24 hours ]

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