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Perineural Catheter Insertion Distance for Continuous Peripheral Nerve Blocks

Phase 4
Completed
Conditions
Lower Extremity Surgery
Upper Extremity Surgery
Post-operative Pain
Interventions
Procedure: Sciatic catheter left 0-1cm past needle tip vs. 5-6cm past needle tip
Registration Number
NCT00997867
Lead Sponsor
University of California, San Diego
Brief Summary

This is a research study to determine if the effects of continuous peripheral nerve blocks are influenced by the distance of insertion past the needle tip of the perineural catheter.

Detailed Description

Specific Aim: Research study to determine the relationships between perineural catheter insertion distance and subsequent continuous peripheral nerve block effects.

Hypothesis: during ultrasound-guided perineural catheter placement, inserting the catheter 0-1cm past the needle tip is associated with decreased postoperative pain compared with inserting the catheter 5-6cm past the needle tip.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
350
Inclusion Criteria
  • undergoing surgery with a planned popliteal perineural catheter for postoperative analgesia
  • age 18 years or older
Exclusion Criteria
  • pregnancy
  • inability to communicate with the investigators and hospital staff
  • incarceration
  • clinical neuropathy in the surgical extremity
  • chronic high-dose opioid use
  • history of opioid abuse

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Catheter 0-1cm past needle tipSciatic catheter left 0-1cm past needle tip vs. 5-6cm past needle tipPatients will be receiving a sciatic (popliteal), femoral, or interscalene nerve block and will be randomized to having the catheter placed 0-1cm past the needle tip. The patient will be called the following day by research staff to assess their post-surgical pain.
Catheter placed 5-6cm past needle tipSciatic catheter left 0-1cm past needle tip vs. 5-6cm past needle tipPatients will be receiving a sciatic (popliteal), femoral, or interscalene nerve block and will be randomized to having the catheter placed 5-6cm past the needle tip. Patients will be called the following day by research staff to assess their post-surgical pain.
Primary Outcome Measures
NameTimeMethod
Average pain in the three hours previous to a phone call the day following surgery as measured on a numeric rating scale (0-10, 0=no pain, 10=worst imaginable pain).Day 1 after surgery, 3 hours prior to phone call
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

UCSD Medical Center

🇺🇸

San Diego, California, United States

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