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Completed

NCT Number: NCT05686395

Pain Control After Arthroscopic Shoulder Surgeries

This study will be conducted to compare the perioperative analgesic efficacy of ultrasound - guided interscalene brachial plexus block versus combined shoulder anterior capsular block and anterior suprascapular nerve block for arthroscopic shoulder surgeries.

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Key information

Conditions

Post Operative Pain Neurologic Manifestations Pain Pain, Postoperative Pathologic Processes Pathological Conditions, Signs and Symptoms Postoperative Complications Signs and Symptoms

Age range

20 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Faculty of Medicine Tanta University

Tanta, Egypt

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients aged 20-65 years of both sexes, with American Society of Anesthesiologists (ASA) physical status I or II admitted for arthroscopic shoulder surgery.

Exclusion criteria

  • Patient refusal.
  • Uncooperative patient.
  • Patient with neurological deficit.
  • Patients with respiratory disorders.
  • Patient with bleeding disorders.
  • Infection at the block injection site.
  • Patients with history of allergy to local anesthetics.

Treatment and study plan

Ultrasound-guided Interscalene Block group

Procedure

ultrasound guided interscalene block versus combined ultrasound guided shoulder anterior capsular block and suprascapular nerve block for arthroscopic shoulder surgery

Combined Ultrasound guided shoulder anterior capsular block and suprascapular nerve block

Procedure

Combined Ultrasound guided shoulder anterior capsular block and suprascapular nerve block

Bupivacaine

Drug

bupivacaine 0.25%.

Primary outcomes

  1. post operative analgesic consumption

    Time frame: 24 hours after surgery

    The first 24 hours post operative analgesic consumption

Secondary outcomes

  1. Visual Analogue score (VAS) in the first 24 hours after surgery

    Time frame: first 24 hours after surgery

    • Postoperative pain intensity will be assessed in the first 24 hour using VAS score where (0 = no pain and 100 = the worst imaginable pain)

  2. Patient satisfaction score

    Time frame: first 24 hours after surgery

    Patient satisfaction score will be assessed on the basis of a questionnaire and graded on a 4-point scale (excellent/good/fair/poor).

  3. The incidence of hemi diaphragmatic paralysis

    Time frame: immediately before block and immediately after procedure

    hemidiaphragmatic paralysis after block

Sponsors and collaborators

Lead sponsor

Tanta University

Other

Registry information

Official study title

Comparative Study of Analgesic Efficacy of Ultrasound Guided Interscalene Block Versus Combined Shoulder Anterior Capsular Block and Suprascapular Nerve Block for Arthroscopic Shoulder Surgeries.

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Jan 17, 2023
Registry last updated
Dec 19, 2024

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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