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Clinical Trials/NCT04941235
NCT04941235
Completed
Not Applicable

The Effectiveness of Different Techniques of Interscalene Brachial Plexus Block With General Anesthesia for Shoulder Arthroscopy

Minia University1 site in 1 country80 target enrollmentMay 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Shoulder and Upper Arm Injury
Sponsor
Minia University
Enrollment
80
Locations
1
Primary Endpoint
Analgesic effect of each technique
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

There are different techniques of interscalene brachial plexus block, we aimed to evaluate the effectiveness of 3 of them as analgesia during shoulder arthroscopy surgery under general anesthesia.

Detailed Description

Prospective randomized controlled study There were 4 groups included in our study: Group N: nerve stimulator guided interscalene brachial plexus block was done Group U: ultrasound guided interscalene brachial plexus block was done Group NU: dual guidance (using both nerve stimulator and ultrasound) Group C: control group We assessed in each group: heart rate, noninvasive blood pressure, time needed for block, onset of sensory and motor power loss and their offset, and finally patient satisfaction.

Registry
clinicaltrials.gov
Start Date
May 1, 2018
End Date
August 31, 2020
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Minia University
Responsible Party
Principal Investigator
Principal Investigator

Shery Shehata Kyriacos

Assistant Lecturer

Minia University

Eligibility Criteria

Inclusion Criteria

  • Age: 18-65 years old.
  • Sex: Both sexes.
  • ASA I \& II.

Exclusion Criteria

  • - Patient refusal.
  • Bleeding disorders.
  • Damage or disease of the brachial plexus.
  • ASA more than II.
  • Pre-existing peripheral neuropathy.
  • Patients with neuromuscular diseases.
  • Patients with known hypersensitivity to drugs of the study.
  • Patients with local skin infection at the site of injection.
  • Psychiatric diseases interfering with evaluation of the block.

Outcomes

Primary Outcomes

Analgesic effect of each technique

Time Frame: 12 hour

using visual analogue scale for pain The patient is asked to express the degree of pain in numbers from 0-10, where 0 means no pain and 10 represents severe pain.

Study Sites (1)

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