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NCT04096144 · ClinicalTrials.gov registry record · Phase 3

Comparison of Sugammadex and Neostigmine During PACU Stay

A Phase 3 study, sponsored by University of South Florida.

Not yet
Registry status
Phase 3
Development phase
50
Enrollment target

NCT04096144 is a Phase 3 study that has not yet begun recruiting, run by University of South Florida. The registered enrollment target is 50 participants.

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The verdict

NCT04096144, a Phase 3 study, has not yet begun recruiting, sponsored by University of South Florida.

NOT YET RECRUITING
Registry status
Phase 3
Development phase
50 participants
Enrollment target

Study Summary

Sugammadex was approved for post-operative use in the operating room (OR) and post-anesthesia recovery unit (PACU) of our quaternary facility, Tampa General Hospital. The approval came with administrative limitations: 2mg/kg dose only and for the first year its utilization was limited as replacement for up to half of Neostigmine/Glycopyrrolate use. An MUE evaluation was completed for a retrospective chart review from March 2017 to December 2017 (10 months) to assess all cases in which patients received Sugammadex or Neostigmine. During the year of data collection, we also noted a widespread tendency to reduce the usage of narcotics. A t-test comparison of the length of stay (LOS) in the PACU revealed a highly significant difference between the LOS in PACU for both drugs. On average, patients receiving Sugammadex were discharged from the PACU 43 minutes earlier than patients who received Neostigmine/Glycopyrrolate. The patient mix in both groups was similar, but these data were obtained retrospectively by a pharmacy chart review.

Interventions

  • DRUG Neuromuscular Blocking Agents

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2019-10-15
Est. Completion 2020-06-15
Phase Phase 3

Sponsor

University of South Florida

252 total trials

What the Registry Record Tells You About NCT04096144

The ClinicalTrials.gov registry entry for NCT04096144 describes a study currently listed as not yet recruiting, categorized as Phase 3. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of South Florida, which has 252 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Neuromuscular Blocking Agents is the first listed.

NCT04096144 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04096144 about?

NCT04096144 is a clinical study titled "Comparison of Sugammadex and Neostigmine During PACU Stay". Sugammadex was approved for post-operative use in the operating room (OR) and post-anesthesia recovery unit (PACU) of our quaternary facility, Tampa General Hospital. The approval came with administrative limitations: 2mg/kg dose only and for the first year its utilization was limited as replacement...

What is the current status of trial NCT04096144?

This trial is currently not yet recruiting. It is a Phase 3 study. The enrollment target is 50 participants. The study started on 2019-10-15. Estimated completion is 2020-06-15.

What interventions are being tested in trial NCT04096144?

The interventions under investigation include: Neuromuscular Blocking Agents (DRUG).

Who is sponsoring clinical trial NCT04096144?

This trial is sponsored by University of South Florida, which has 252 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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.