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Clinical Trials/NCT06500572
NCT06500572
Completed
N/A

Ultrasound Guided, Landmark Guided Intercostobrachial Nerve Block Versus Serratus Plane Block After Supraclavicular Plexus Block for Anesthesia in Creation of Arteriovenous Fistula in the Medial Side of the Arm: A Randomized Trial

Tanta University1 site in 1 country75 target enrollmentJuly 13, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Intercostobrachial Nerve Block
Sponsor
Tanta University
Enrollment
75
Locations
1
Primary Endpoint
Percent of patients who needed local anesthetic supplementation
Status
Completed
Last Updated
last year

Overview

Brief Summary

This study aims to compare the role of ultrasound-guided and landmark-guided intercostobrachial nerve block and serratus plane block after supraclavicular plexus block for anesthesia in the creation of an arteriovenous fistula in the medial side of the arm.

Detailed Description

Brachial plexus block (BPB) is usually utilized for proximal arm arteriovenous access creation. It has been suggested that supraclavicular brachial plexus block (SCPB) could be an alternative and provide comparable effective anesthesia and postoperative analgesia for arm surgery, with a reduced incidence of adverse events, including hemidiaphragmatic paresis. By performing SCPB, the inner part of the arm is not completely anesthetized because this part of the arm is innervated by the lateral cutaneous branch of the second intercostal nerve (intercostobrachial nerve (ICBN)) and the medial branch of the brachial cutaneous nerve. Serratus plane block (SPB) was first defined in 2013 by Blanco et al. This block provides anesthesia and analgesia in the hemi-thorax, where it is applied to block the thoracic intercostal nerves, in addition to the axillary region and shoulder posteriorly.

Registry
clinicaltrials.gov
Start Date
July 13, 2024
End Date
February 27, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mohamed Zakarea Wfa

Lecturer of Anesthesiology, Surgical Intensive Care and Pain Medicine, Faculty of Medicine, Tanta University, Tanta, Egypt

Tanta University

Eligibility Criteria

Inclusion Criteria

  • Age from 18 to 65 years.
  • Both sexes.
  • American Society of Anesthesiology (ASA) physical status I-II.
  • Scheduled for creation of arteriovenous fistula in the medial side of the arm.

Exclusion Criteria

  • Allergy to local anesthetics.
  • Drug addiction.
  • Coagulation abnormalities.
  • Body Mass Index (BMI)≥35 kg/m
  • Upper extremity neuropathy.
  • Vasculitis.
  • Unstable hemodynamics.
  • History of seizures or mental illness.
  • Severe heart, kidney, and liver diseases.
  • Pregnancy.

Outcomes

Primary Outcomes

Percent of patients who needed local anesthetic supplementation

Time Frame: Intraoperatively

Number of patients who needed local anesthetic supplementation will be recorded.

Secondary Outcomes

  • Total amount of morphine consumption(24 hours postoperatively)
  • Patient satisfaction(24 hours postoperatively)

Study Sites (1)

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