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Completed

NCT Number: NCT06055478

Effect of Suprascapular Nerve Block and Axillary Nerve Block After Arthroscopic Rotator Cuff Repair

The goal of this clinical trial is to verify the effect of suprascapular nerve block and axillary nerve block in relieving postoperative pain after arthroscopic rotator cuff repair.

Are there differences in visual analog pain scale and patient's satisfaction? Are there differences in mean plasma pain related cytokines? The participants will undergo preemptive ultrasound guided suprascapular nerve block and axillary nerve block using each 0.75% ropivacaine 10mL or each 0.9% saline 10mL.

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Key information

Age range

20 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Jung-Taek Hwang

Chuncheon, Gangwon-do, 24253, South Korea

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • a definite rotator cuff tear that needed repair seen on preoperative magnetic resonancce imaging (MRI)
  • acceptance of arthroscopic surgery including rotator cuff repair
  • age same as or more than 20 years
  • acceptance of preemptive regional block and PCA, and blood testing

Exclusion criteria

  • did not undergo arthroscopic rotator cuff repair
  • stopped PCA before 48 hours postoperatively because of associated side effects
  • a history of previous ipsilateral shoulder operation or fracture
  • a concomitant neurologic disorder around the shoulder
  • a failure of blood sampling including hemolysis, etc.

Treatment and study plan

Preemptive ultrasound-guided suprascapular nerve block and axillary nerve block

Procedure

Preemptive ultrasound-guided suprascapular nerve block and axillary nerve block using ropivacaine or saline.

Low fixed dose patient controlled analgesia (PCA) were done in the two group.

Other names: a low fixed dose patient controlled analgesia (PCA)

Primary outcomes

  1. visual analog pain scale (VAS)

    Time frame: preoperative, postoperative 1, 3, 6, 12, 18, 24, 36, 48 hour(s)

    0-10, 0: no pain, 10: very severe pain

Secondary outcomes

  1. Patient's satisfaction (SAT)

    Time frame: preoperative, postoperative 1, 3, 6, 12, 18, 24, 36, 48 hour(s)

    0-10, 0: not satisfied, 10: very much satisfied

  2. IL-6

    Time frame: preoperative, postoperative 1, 6, 12, 24, 48 hour(s)

    pg/mL

  3. IL-8

    Time frame: preoperative, postoperative 1, 6, 12, 24, 48 hour(s)

    pg/mL

  4. IL-1β

    Time frame: preoperative, postoperative 1, 6, 12, 24, 48 hour(s)

    pg/mL

  5. Substance P

    Time frame: preoperative, postoperative 1, 6, 12, 24, 48 hour(s)

    pg/mL

  6. Serotonin

    Time frame: preoperative, postoperative 1, 6, 12, 24, 48 hour(s)

    ng/mL

  7. β -endorphin

    Time frame: preoperative, postoperative 1, 6, 12, 24, 48 hour(s)

    pg/mL

  8. norepinephrine

    Time frame: preoperative, postoperative 1, 6, 12, 24, 48 hour(s)

    pg/mL

Sponsors and collaborators

Lead sponsor

Chuncheon Sacred Heart Hospital

Other

Collaborators

  • Hallym University Medical Center

Registry information

Official study title

Effect of Ultrasound-guided Suprascapular Nerve Block and Axillary Nerve Block in Relieving Postoperative Pain After Arthroscopic Rotator Cuff Repair

Important dates

Study start
2023
Primary completion
2024
Study completion
2025
First posted
Sep 26, 2023
Registry last updated
Aug 20, 2026

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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