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

Sponsor
VA Palo Alto Health Care System (U.S. Fed)
Overall Status
Completed
CT.gov ID
NCT01459523
Collaborator
(none)
200
1
2
31
6.5

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Proximal placement
  • Procedure: Short axis ultrasound
  • Procedure: Long axis
  • Procedure: Distal placement
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Optimizing Catheter Insertion Technique for Ultrasound-guided Continuous Peripheral Nerve Blocks
Study Start Date :
Oct 1, 2011
Actual Primary Completion Date :
Apr 1, 2014
Actual Study Completion Date :
May 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Imaging technique

In one substudy, subjects will be randomly assigned to either short axis or long axis target ultrasound imaging for perineural catheter insertion. The onset time of sensory anesthesia will be measured following local anesthetic bolus via the catheter.

Procedure: Short axis ultrasound
Subjects assigned to this group will have the target nerve or plexus identified in short axis (cross-section) using ultrasound. Perineural catheter insertion will be performed in-plane. The onset time of sensory anesthesia will be measured following local anesthetic bolus via the catheter.
Other Names:
  • Perineural catheter
  • Ultrasound
  • Catheter placement technique
  • Procedure: Long axis
    Subjects assigned to this group will have the target nerve or plexus identified in long axis (longitudinal) using ultrasound. Perineural catheter insertion will be performed in-plane. The onset time of sensory anesthesia will be measured following local anesthetic bolus via the catheter.
    Other Names:
  • Perineural catheter
  • Ultrasound
  • Catheter placement technique
  • Active Comparator: Catheter location

    In another substudy, subjects will be randomly assigned to receive their perineural catheters either proximally or distally along the same target nerve or plexus.

    Procedure: Proximal placement
    Subjects assigned to this group will have their perineural catheter placed in a proximal position (higher up in the arm or leg) with ultrasound guidance. The onset time of sensory anesthesia will be measured following local anesthetic bolus via the catheter.
    Other Names:
  • Perineural catheter
  • Ultrasound
  • Catheter placement technique
  • Procedure: Distal placement
    Subjects assigned to this group will have their perineural catheter placed in a distal position (further down in the arm or leg) with ultrasound guidance. The onset time of sensory anesthesia will be measured following local anesthetic bolus via the catheter.
    Other Names:
  • Perineural catheter
  • Ultrasound
  • Catheter placement technique
  • Outcome Measures

    Primary Outcome Measures

    1. Onset time of sensory anesthesia [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 Outcome Measures

    1. Time for placement [30 minutes]

      A secondary outcome measure will be the time required to insert the perineural catheter using the technique or location assigned.

    2. Postoperative pain [1 day]

      A secondary outcome will be the surgical pain experienced by subjects as assessed by a 0-10 scale (0=no pain; 10=worst pain imaginable) and amount of opioid medications consumed.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion criteria:
    • At least 18 years of age;

    • Undergoing unilateral, upper (at or distal to the elbow) or lower (hip or distal) extremity orthopedic surgery, with moderate-to-severe postoperative pain expected; and

    • Desiring a continuous perineural catheter for postoperative analgesia.

    Exclusion criteria:
    • Patients who will have difficulty understanding the study protocol or caring for the infusion pump/catheter system; or

    • Patients with any known contraindication to study medications, insulin-dependent diabetes mellitus, neuropathy of any etiology in the affected extremity;

    • Patients with a contraindication to regional blockade (eg, clotting deficiency);

    • Patients with any known acute or chronic hepatic or renal insufficiency or failure;

    • Patients with any additional surgical site outside of the catheter-affected area (eg, iliac crest bone graft in addition to hand surgery);

    • Patients with chronic opioid use (defined as daily use for more than 4 weeks prior to surgery) or active illicit substance abuse;

    • Patient weighing < 40 kg;

    • Pregnancy;

    • Incarceration; or

    • Inability to communicate with the investigators and hospital staff.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 VA Palo Alto Health System Palo Alto California United States 94304

    Sponsors and Collaborators

    • VA Palo Alto Health Care System

    Investigators

    • Principal Investigator: Edward R Mariano, MD, MAS, VA Palo Alto Health Care System (VAPAHCS)

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Edward R. Mariano, Staff Physician, VA Palo Alto Health Care System
    ClinicalTrials.gov Identifier:
    NCT01459523
    Other Study ID Numbers:
    • 21961
    First Posted:
    Oct 25, 2011
    Last Update Posted:
    May 4, 2021
    Last Verified:
    Apr 1, 2021
    Keywords provided by Edward R. Mariano, Staff Physician, VA Palo Alto Health Care System
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 4, 2021