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Availability of Lipid Emulsion to Regional Anesthesia Programs at US Academic Anesthesia Departments

Availability of Lipid Emulsion to Regional Anesthesia Programs at US Academic Anesthesia Departments

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01880034
Enrollment
18
Registered
2013-06-18
Start date
2013-06-30
Completion date
2014-12-31
Last updated
2017-05-12

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

Conditions

Local Anesthetic Systemic Toxicity

Brief summary

Significant data exists to suggest that lipid emulsion administration in the setting of local anesthetic toxicity has the potential to be life-saving. Unfortunately, a variety of potential barriers exist to routine lipid emulsion administration for those performing regional anesthesia including drug availability, drug cost and drug location. Inadequate training or lack of established protocols also have the potential to negatively impact patient outcomes. A previous study by Toledo et al (Availability of lipid emulsion in United States obstetric units. Anesth Analg 2013;116:406-408.) evaluated lipid emulsion availability on obstetric units and found that it was nearly universally available. The Accreditation Council for Graduate Medical Education (ACGME) publishes a list of contact information for each anesthesia institution that engages in resident training. Investigators will contact these institutions by phone or email to obtain contact information for their regional anesthesia program director. In the absence of a program director, investigators will send a survey and consent information via email to the faculty physician most involved in regional anesthesia. Survey completion instructions (survey itself to be completed on Qualtrics Survey Hosting Service) and copy of the study consent form will be attached to the initial contact email. The study consent form will contain a description of the study itself. Survey participants will be allowed time to complete their survey in private at their discretion. Non-responders will receive two follow-up emails at one month intervals.

Interventions

OTHERLipid Emulsion Survey

Sponsors

University of Wisconsin, Madison
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Regional Anesthesia Section heads at academic anesthesia institutions.

Design outcomes

Primary

MeasureTime frameDescription
Is lipid emulsion available at all locations where regional anesthesia is practiced in your institution?Two monthsSurvey options include 1. Yes, lipid emulsion is available in the room where regional anesthesia is performed. 2. Yes, lipid emulsion is available in a near-by pharmacy 3. Yes, lipid emulsion is available in a central pharmacy 4. No, lipid emulsion is not available in all locations where regional anesthesia is performed

Secondary

MeasureTime frameDescription
If lipid emulsion is available to those practicing regional anesthesia at your institution, how long would it take to obtain it?Two Months.Possible responses include: * Lipid emulsion is not available at our institution. * Less than 10 minutes * 10-30 minutes * More than 30 minutes

Countries

United States

Outcome results

None listed

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