Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01094119 · ClinicalTrials.gov registry record · NA
A Randomized Comparison of Intraoperative Warming With the LMA PerfecTemp and Forced-air
A NA study, sponsored by The Cleveland Clinic.
- Completed
- Registry status
- NA
- Development phase
- 70
- Enrollment target
NCT01094119 is a NA study that has completed, run by The Cleveland Clinic. The registered enrollment target is 70 participants.
The verdict
NCT01094119, a NA study, has completed, sponsored by The Cleveland Clinic.
- COMPLETED
- Registry status
- NA
- Development phase
- 70 participants
- Enrollment target
Study Summary
Recently, a novel posterior heating system has been developed that provides enhanced pressure relief: the Laryngeal Mask Airway (LMA) PerfecTemp. Anactodal experience with this FDA-approved system suggests that the PerfecTemp warmer is effective, even in open abdominal surgery. The investigators therefore propose to test the hypothesis that intraoperative distal esophageal (core) temperatures with PerfecTemp warming are non-inferior to upper-body forced-air warming in patients undergoing open major abdominal surgery under general anesthesia. Secondary hypotheses include that: 1. intraoperative core temperatures are superior with PerfecTemp than upper-body forced-air warming 2. final intraoperative core temperature is non-inferior with PerfecTemp than upper-body forced-air warming 3. final intraoperative core temperature is superior with PerfecTemp than upper-body forced-air warming.
Interventions
- DEVICE heated blanket
- DEVICE heated pad
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 70 participants |
| Start Date | 2010-03 |
| Est. Completion | 2010-08 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01094119
The ClinicalTrials.gov registry entry for NCT01094119 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 70 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The Cleveland Clinic, which has 688 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which heated blanket is the first listed.
NCT01094119 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01094119 about?
NCT01094119 is a clinical study titled "A Randomized Comparison of Intraoperative Warming With the LMA PerfecTemp and Forced-air". Recently, a novel posterior heating system has been developed that provides enhanced pressure relief: the Laryngeal Mask Airway (LMA) PerfecTemp. Anactodal experience with this FDA-approved system suggests that the PerfecTemp warmer is effective, even in open abdominal surgery. The investigators the...
What is the current status of trial NCT01094119?
This trial is currently completed. It is a NA study. The enrollment target is 70 participants. The study started on 2010-03. Estimated completion is 2010-08.
What interventions are being tested in trial NCT01094119?
The interventions under investigation include: heated blanket (DEVICE), heated pad (DEVICE).
Who is sponsoring clinical trial NCT01094119?
This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.