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Paravertebral Block With Brachial Plexus Block for Upper Arm Arteriovenous Fistula Surgery

Not Applicable
Completed
Conditions
Regional Anesthesia Success
Interventions
Procedure: T2 paravertebral nerve block
Procedure: Subcutaneous infiltration of intercostobrachial nerve
Registration Number
NCT04720079
Lead Sponsor
University of North Carolina, Chapel Hill
Brief Summary

The primary goal of this quality improvement project is to find the optimal surgical conditions for patients undergoing upper arm arteriovenous graft surgery. Currently, there are two anesthetic techniques used in clinical practice. The goal is to standardize future practice and improve the care of patients postoperatively. The two techniques used in conjunction with a brachial plexus block are paravertebral nerve block and subcutaneous infiltration.

Detailed Description

This study is designed to test the null hypothesis that paravertebral nerve block or subcutaneous infiltration provide similar operating conditions when combined with supraclavicular nerve block for upper arm arteriovenous fistula surgery. The results will help determine which approach to use and guide future research in this area.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
63
Inclusion Criteria
  • Adult patients (>18 years) undergoing upper limb arteriovenous fistula surgery at UNC Chapel Hill hospital
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Exclusion Criteria
  • Contraindication to regional anesthesia
  • Significant peripheral neuropathy or neurological disorder of the upper extremity
  • Cognitive or psychiatric condition that will interfere with patient assessment
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Ultrasound guided T2 paravertebral blockT2 paravertebral nerve blockPreoperative ultrasound guided T2 paravertebral nerve block with 10ml of ropivacaine 0.5%
Intercostobrachial nerve InfiltrationSubcutaneous infiltration of intercostobrachial nervePreoperative infiltration of intercostobrachial nerve with 10ml of ropivacaine 0.5%
Primary Outcome Measures
NameTimeMethod
Number of Participants with Successful Regional AnesthesiaBy end of surgery

Success is considered a regional anesthetic without rescue analgesic medications (including surgeon administered local anesthetic) or conversion to general anesthesia

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of North Carolina at Chapel Hill

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Chapel Hill, North Carolina, United States

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