Skip to content

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

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

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01221415
Enrollment
0
Registered
2010-10-15
Start date
2008-01-31
Completion date
2011-10-31
Last updated
2022-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Orthopedic

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.

Interventions

None listed

Sponsors

Ochsner Health System
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
time from injection of local anesthetic to adequate surgical anesthesiawithin the first 45 minutes after injection of local anesthestic

Secondary

MeasureTime frame
effectiveness of blockwithin 1 hour of injection
time taken to locate the target nerve and inject local anestheticwithin 45 minutes prior to 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

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026