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A Comparison of Ultrasound and Nerve Stimulator Techniques for Nerve Localization in Regional Anesthesia

Withdrawn
Conditions
Orthopedic
Registration Number
NCT01221415
Lead Sponsor
Ochsner Health System
Brief Summary

The primary objective of this study is to compare ultrasound versus nerve stimulator techniques for nerve localization when performing peripheral nerve blocks. Specifically the investigators will be performing Popliteal, Femoral, and Interscalene nerve blocks. The investigators will be looking for differences in 1) time taken to locate the target nerve and inject local anesthetic 2) time from injection of local anesthetic to adequate surgical anesthesia 3) effectiveness of block 4) incidence of vascular puncture 5) incidence of adverse events 6) patient satisfaction.

Detailed Description

After obtaining informed consent, subjects will be randomized to either the ultrasound or nerve stimulator groups as the method for nerve localization prior to peripheral block placement.

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • American Society of Anesthesiologists (ASA) Physical status I-III
  • Arthroscopic knee surgery or Lower leg/foot surgery as well as shoulder arthroscopy
  • Outpatient status
  • Patient preference for a regional anesthetic
  • Subjects should be capable of giving informed consent
Exclusion Criteria
  • Allergy to:

    • Local anesthetics
    • Hydromorphone
    • Propofol
    • Midazolam
  • Patient refusal

  • Infection at the injection site

  • Peripheral Neuropathy

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
time from injection of local anesthetic to adequate surgical anesthesiawithin the first 45 minutes after injection of local anesthestic
Secondary Outcome Measures
NameTimeMethod
time taken to locate the target nerve and inject local anestheticwithin 45 minutes prior to injection
effectiveness of blockwithin 1 hour of injection
incidence of vascular puncturewithin 30 minutes of injection
incidence of adverse eventswithin 2 weeks of the day of surgery
patient satisfactionwithin 2 weeks of the date of surgery

Trial Locations

Locations (1)

Ochsner Clinic Foundation

🇺🇸

New Orleans, Louisiana, United States

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