Sponsor study identifier
observational
18
1 country
1
Study Start
June 2013
Date type not reportedThis date has not been verified as actual or estimated.
Primary Completion
December 2014
Actual (reported)Study Completion
December 2014
Actual (reported)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.
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
December 2014
Actual (reported)Click on a node to explore related trials.
Some registry-reported names shown below are not yet linked in this graph.
Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
June 2013
Date type not reportedThis date has not been verified as actual or estimated.
June 13, 2013
Actual (reported)June 18, 2013
Actual (reported)December 2014
Actual (reported)December 2014
Actual (reported)Is lipid emulsion available at all locations where regional anesthesia is practiced in your institution?
Survey 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
Two months
If lipid emulsion is available to those practicing regional anesthesia at your institution, how long would it take to obtain it?
Two Months.
This group will consist of Regional Anesthesia Section Heads at anesthesia residency training programs.
Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.
Regional Anesthesia Section heads at academic anesthesia institutions.
Contact the study team to confirm eligibility.
University of Wisconsin School of Medicine and Public Health
Madison, Wisconsin, 53792, United States
18 participants (actual enrollment reported by the registry).
First Submitted
June 13, 2013
First Posted
June 18, 2013
Study Start
June 2013
Date type not reportedThis date has not been verified as actual or estimated.
Primary Completion
December 2014
Actual (reported)Study Completion
December 2014
Actual (reported)Last Updated
May 12, 2017
Record last verified: 2017-05
Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.
Source: ClinicalTrials.gov.
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