Skip to main content
Clinical Trials/NCT01459523
NCT01459523
Completed
Not Applicable

Optimizing Catheter Insertion Technique for Ultrasound-guided Continuous Peripheral Nerve Blocks

VA Palo Alto Health Care System1 site in 1 country200 target enrollmentOctober 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain, Postoperative
Sponsor
VA Palo Alto Health Care System
Enrollment
200
Locations
1
Primary Endpoint
Onset time of sensory anesthesia
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Continuous peripheral nerve blocks (CPNB; also known as "perineural" catheters) provide target-specific pain control for a variety of surgeries. There has been increasing interest in the use of ultrasound guidance for regional anesthesia, and many techniques using ultrasound alone for perineural catheter insertion have been described. Catheters may be placed at various points along the brachial plexus (for upper extremity procedures) or in proximity to the femoral and/or sciatic nerve (for lower extremity procedures). To date, the optimal ultrasound scanning technique, catheter insertion endpoint, catheter placement location per indication, for the majority of ultrasound-guided continuous peripheral nerve blocks remain unknown. This study will help provide important information related to optimal ultrasound scanning techniques and will help identify ways to improve the success rates, onset times, and analgesic effectiveness of these techniques for real patients undergoing surgical procedures.

Detailed Description

Primary Aim: To determine if there is an optimal scanning technique for ultrasound-guided perineural catheter insertion that will result in the most accurate tip placement in proximity to the target nerve or plexus. Secondary Aim: To determine if there is an optimal location for ultrasound-guided perineural catheter insertion along a target nerve or plexus that will result in maximum local anesthetic infusion benefits.

Registry
clinicaltrials.gov
Start Date
October 2011
End Date
May 2014
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
VA Palo Alto Health Care System
Responsible Party
Principal Investigator
Principal Investigator

Edward R. Mariano

Staff Physician

VA Palo Alto Health Care System

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Onset time of sensory anesthesia

Time Frame: 30 minutes

The primary outcome will be the onset time of sensory anesthesia in the target nerve distribution following injection of a local anesthetic bolus via the perineural catheter.

Secondary Outcomes

  • Time for placement(30 minutes)
  • Postoperative pain(1 day)

Study Sites (1)

Loading locations...

Similar Trials