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NCT Number: NCT06765278

Anterior Glenoid Nerve Block Versus Pericapsular Nerve Group Block Versus Interscalene Brachial Plexus Block for Postoperative Pain Management in Shoulder Arthroscopic Surgeries

This study aims to compare between Anterior glenoid nerve block, pericapsular nerve group (PENG) block and Interscalene brachial plexus (ISB) block for post-operative pain management in shoulder arthroscopic surgeries

Recruiting

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ain Shams University

Cairo, 11591, Egypt

Location status: Recruiting

Location contact

Amr E Abd El-Hamid, MD

SUB_INVESTIGATOR

Amr H Ali, MD

SUB_INVESTIGATOR

Ihab H Attia, MD

SUB_INVESTIGATOR

Mohamed Serry, Master

CONTACT

[email protected]

00201002609476

Ossama M Farrag, MD

SUB_INVESTIGATOR

About this study

Major surgeries of the shoulder constitute some of the most commonly performed orthopedic procedures. They often result in moderate to severe postoperative pain thereby requiring a multimodal analgesic approach centered around peripheral nerve blocks.

Postoperative pain management is the part of shoulder surgery to improve patient satisfaction, start rehabilitation process rapidly and decrease for hospital stay.

Interscalene blocks (ISB) are well-studied and established means of providing analgesia following shoulder surgery and are considered the gold standard mode of regional anesthesia and post-operative pain management in shoulder surgeries.

A novel technique: pericapsular nerve group (PENG) block can be effectively and safely applied under ultrasound guidance in shoulder surgery cases for postoperative analgesia. In addition, PENG block targets articular branches with less motor effect compared with interscalene brachial plexus block providing anesthetic and analgesic effect with less complication and better and sooner ambulation.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age from 18 to 70 years.
  • No sex predilection.
  • American Society of Anesthesiology (ASA) physical status I-II.
  • Undergoing shoulder arthroscopic surgeries.

Exclusion criteria

  • Patient's refusal.
  • Patients with a history of drug allergies to study drugs.
  • Evidence of local infection at the site of injection.
  • Inability to cooperate
  • Neuromuscular pathology (example: - Multiple Sclerosis)
  • Previous trauma or surgery to the shoulder

Treatment and study plan

Interscalene brachial plexus block

Other

Patients will receive an Interscalene brachial plexus block.

Anterior glenoid nerve block

Other

Patients will receive an anterior glenoid nerve block.

Pericapsular nerve group block

Other

Patients will receive a pericapsular nerve group (PENG) block.

Primary outcomes

  1. Time to the 1st rescue analgesia

    Time frame: 24 hours postoperatively

    Time to the first request for the rescue analgesia (time from the end of surgery to the first dose of pethidine administrated).

Secondary outcomes

  1. Total pethidine consumption

    Time frame: 24 hours postoperatively

    All patients will receive intravenous pethidine (30mg) on demand [Visual Analogue Scale (VAS) score ≥3].

  2. Degree of pain

    Time frame: 24 hours postoperatively

    Degree of pain will be assessed using visual analogue scale (VAS). Each patient will be instructed about postoperative pain assessment with the VAS. VAS (0 represents "no pain" while 10 represents "the worst pain imaginable"). VAS will be assessed at 0, 6, 12, and 24 hours postoperatively.

  3. Length of hospital stay

    Time frame: Till discharge from hospital (Up to one week).

    Length of hospital stay will be recorded from admission till the discharge from hospital.

  4. Time needed for the patient to freely move the operated limb

    Time frame: Postoperatively (Up to one week).

    Time needed for the patient to freely move the operated limb will be recorded.

  5. Degree of patients satisfaction

    Time frame: 24 hours postoperatively

    Degree of patient satisfaction will be assessed on a 5-point Likert scale patient satisfaction (1, extremely dissatisfied; 2, unsatisfied; 3, neutral; 4, satisfied; 5, extremely satisfied)

Study contacts

Contact information is provided by the study sponsor or research team.

Mohamed Serry, Master

CONTACT

[email protected]

00201002609476

Sponsors and collaborators

Lead sponsor

Ain Shams University

Other

Registry information

Official study title

Anterior Glenoid Nerve Block Versus Pericapsular Nerve Group (PENG) Block Versus Interscalene Brachial Plexus (ISB) Block for Postoperative Pain Management in Shoulder Arthroscopic Surgeries

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Jan 9, 2025
Registry last updated
Jan 14, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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