Skip to main content
Clinical Trials/NCT04669639
NCT04669639CompletedNot Applicable

A Comparison of Erector Spinae Plane Block to Suprascapular Nerve Block for Analgesia in Shoulder Surgery

Zagazig University1 site in 1 country96 target enrollmentStarted: December 20, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
96
Locations
1
Primary Endpoint
Intraoperative analgesia

Study Overview

Brief Summary

A comparison between Erector Spinae Plane block and Suprascapular nerve block in providing analgesia for shoulder surgery

Detailed Description

Suprascapular nerve block is considered a phrenic nerve sparing approach that recently introduced as alternative for interscalene brachial plexus nerve block in shoulder surgery. However, some researchers reported that Suprascapular nerve block alone results in an ineffective analgesia. Erector Spinae Plane block is supposed to be able in providing adequate analgesia in shoulder surgery

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Double (Care Provider, Outcomes Assessor)

Masking Description

The care provider and outcome assessor will be unaware of the study design

Eligibility Criteria

Ages
21 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •ASA I and II,
  • •Age above 21 years and below 60 years in both sexes,
  • •Cooperative patients,
  • •Patients with a BMI (body mass index) not exceeding 35.

Exclusion Criteria

  • •patients with cardiovascular or respiratory compromise,
  • •Patient refusal,
  • •Coagulopathy,
  • •Local tissue infection,
  • •Allergy to local anesthesia,
  • •prior to cervical or thoracic spine surgery.

Arms & Interventions

The block group (a)

Experimental

Patients were randomized in a 1:1 :1ratio, group (a) will receive SSN. The nerve blocks The procedure will be performed after induction of anaesthesia and endotracheal intubation.

Intervention: Block procedures for shoulder surgery analgesia (Other)

The block group (b)

Experimental

Patients were randomized in a 1:1:1 ratio. group (b) will receive the Erector spinae plane block. The procedure will be performed after induction of anesthesia and endotracheal intubation.

Intervention: Block procedures for shoulder surgery analgesia (Other)

control group

Placebo Comparator

Patients were randomized in a 1:1:1 ratio. this group will receive general anesthesia (GA) only

Intervention: Block procedures for shoulder surgery analgesia (Other)

Outcomes

Primary Outcomes

Intraoperative analgesia

Time Frame: The intraoperative patients' hemodynamics every 30 min were collected and analyzed till the end of surgery . Also the total dose of opioids consumed intraoperatively will be recorded. Postoperative consumed opioid for 24 hours also will calculated

Recording of the patients' hemodynamics (heart rate and non-invasive blood pressure) and total dose of opioids consumption intraoperatively and postoperatively.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other Gov
Responsible Party
Principal Investigator
Principal Investigator

Naglaa Fathy Abdelhaleem Abdelhaleem

Lecturer, Anesthesia and Surgical Intensive Care department, Faculty of Medicine

Zagazig University

Study Sites (1)

Loading locations...

Similar Trials

A Comparison of ESP Block to SSN Block for... | Clinical Trial