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Completed

NCT Number: NCT03212443

Combined Suprascapular and Axillary Nerve Blocks for Arthroscopic Shoulder Surgery

Arthroscopic shoulder surgery is associated with severe pain postoperatively. Regional nerve block adding to general anesthesia might improve the quality of postoperative analgesia. The aim of the study is to compare the subacromial local anesthetic infiltration and the suprascapular-axillary nerve blocks combination for intraoperative sevoflurane consumption, postoperative analgesia and analgesic consumption.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Derya Ozkan

Ankara, 06110, Turkey (Türkiye)

About this study

After informed consent and with ethics approval, 60 ASA 2-3 patients scheduled for elective arthroscopic shoulder surgery will be included in this study. Patient will be divided to two groups by using computer -generated list for randomization. In group A, the surgeon will apply 20 ml of 0.250% bupivacaine to the subacromial region at the end of the procedure. In Group B, suprascapular (10 ml of 0.250% bupivacaine ) and axillary block (10 ml of 0.250% bupivacaine) will be performed with ultrasound and nerve stimulator guidance before induction of anesthesia. In all patients after standard and BIS (Bi spectral index) monitorization general anesthesia will be induced with remifentanil (10mcg iv), propofol (2.5 mg/kg iv) and rocuronium (0.5mg/kg iv). After intubation, anesthesia will be maintained with 50% O2 and N2O mixture. Hemodynamic parameters, BIS values, end-tidal sevoflurane consumption will be recorded by blind investigator. Postoperative visual analog scale (VAS) values, postoperative analgesic consumption (Tramadol, patient controlled analgesia), complications will be recorded.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • American society of anesthesia physical status (ASA) 1,2 patients
  • Elective arthroscopic shoulder surgery

Exclusion criteria

  • ASA 3,4 patients
  • Coagulation abnormality
  • Body mass index >30
  • Preexisting neurological deficit Local anesthetic allergy history Diabetes

Treatment and study plan

Suprascapular nerve- axillary nerve block combination

Procedure

In Group B, suprascapular (10 ml of 0.250% bupivacaine ) and axillary block (10 ml of 0.250% bupivacaine) will be performed with ultrasound and nerve stimulator guidance before induction of anesthesia

Subacromial infiltration

Procedure

In group A, the surgeon will apply 20 ml of 0.250% bupivacaine to the subacromial region at the end of the procedure

Primary outcomes

  1. Postoperative VAS scores

    Time frame: Through postoperative period, an avarage of 30 minutes

    Ranging from 0: no pain to 10: worst pain

Secondary outcomes

  1. sevoflurane consumption

    Time frame: 5th, 10th,20th,30th,40th,50th minutes after induction of anesthesia

    End tidal sevoflurane concentration values assesment during the surgery

Other outcomes

  1. Bleeding assesment

    Time frame: 5th, 10th,20th,30th,40th,50th minutes after induction of anesthesia

    stage1: Good surgical visualization (numeric rating scale 7<), Stage 2: Moderate bleeding (numeric rating sacle =4-7), Stage 3: Severe bleeding, bad surgical visualization (numeric rating scale < 4)

Sponsors and collaborators

Lead sponsor

Diskapi Teaching and Research Hospital

Other

Registry information

Official study title

Combined Suprascapular and Axillary Nerve Blocks for Sevoflurane Consumption and Postoperative Analgesia in Arthroscopic Shoulder Surgery

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Jul 11, 2017
Registry last updated
Aug 7, 2018

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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