Clinical Trial

Comparison of Sugammadex and Neostigmine During PACU Stay

Not Yet Recruiting Phase 3
View on ClinicalTrials.gov →
Record status
This record was last updated September 19, 2019 (before its estimated March 1, 2020 completion). Its status may not reflect the trial's current state.
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.
Protocol Amendment History 5 amendments
This ClinicalTrials.gov record has been amended 5 times since 2019-09-17; most recent amendment 2022-05-22.
Status change: Not Yet Recruiting → Completed 2021-11-04
Trial Details
NCT Number NCT04096144
Lead Sponsor University of South Florida
Conditions Neuromuscular Blockade
Enrollment 50 participants
Start Date 2019-10-15
Primary Completion 2020-03-01 (estimated)
Study Completion 2020-06-15 (estimated)
Updated on ClinicalTrials.gov 2019-09-19