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OpenTrials
Completed

NCT Number: NCT01880034

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

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.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Wisconsin School of Medicine and Public Health

Madison, Wisconsin, 53792, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Regional Anesthesia Section heads at academic anesthesia institutions.

Treatment and study plan

Lipid Emulsion Survey

Other

Primary outcomes

  1. Is lipid emulsion available at all locations where regional anesthesia is practiced in your institution?

    Time frame: Two months

    Survey options include

    • Yes, lipid emulsion is available in the room where regional anesthesia is performed.
    • Yes, lipid emulsion is available in a near-by pharmacy
    • Yes, lipid emulsion is available in a central pharmacy
    • No, lipid emulsion is not available in all locations where regional anesthesia is performed

Secondary outcomes

  1. If lipid emulsion is available to those practicing regional anesthesia at your institution, how long would it take to obtain it?

    Time frame: Two Months.

    Possible responses include:

    • Lipid emulsion is not available at our institution.
    • Less than 10 minutes
    • 10-30 minutes
    • More than 30 minutes

Sponsors and collaborators

Lead sponsor

University of Wisconsin, Madison

Other

Registry information

Important dates

Study start
2013
Primary completion
2014
Study completion
2014
First posted
Jun 18, 2013
Registry last updated
May 12, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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