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NCT01880034 · ClinicalTrials.gov registry record
Availability of Lipid Emulsion to Regional Anesthesia Programs at US Academic Anesthesia Departments
A clinical trial, sponsored by University of Wisconsin, Madison.
- Completed
- Registry status
- 18
- Enrollment target
NCT01880034 is a clinical trial that has completed, run by University of Wisconsin, Madison. The registered enrollment target is 18 participants.
The verdict
NCT01880034 has completed, sponsored by University of Wisconsin, Madison.
- COMPLETED
- Registry status
- 18 participants
- Enrollment target
Study 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
- OTHER Lipid Emulsion Survey
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 18 participants |
| Start Date | 2013-06 |
| Est. Completion | 2014-12 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01880034
The ClinicalTrials.gov registry entry for NCT01880034 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 18 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Wisconsin, Madison, which has 1,039 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Lipid Emulsion Survey is the first listed.
NCT01880034 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01880034 about?
NCT01880034 is a clinical study titled "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...
What is the current status of trial NCT01880034?
This trial is currently completed. The enrollment target is 18 participants. The study started on 2013-06. Estimated completion is 2014-12.
What interventions are being tested in trial NCT01880034?
The interventions under investigation include: Lipid Emulsion Survey (OTHER).
Who is sponsoring clinical trial NCT01880034?
This trial is sponsored by University of Wisconsin, Madison, which has 1,039 total clinical trials registered on ClinicalTrials.gov.
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