Can a smaller dose of sugammadex rescue patients when standard reversal fails?
NCT ID NCT05661409
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tested five different low doses of sugammadex (a drug that reverses muscle relaxants) in 46 adults who still had muscle weakness after the standard reversal drug neostigmine. The goal was to see how quickly each dose restored normal muscle function. If a lower dose works, it could give doctors more options and reduce side effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- sugammadex
- What this could lead to
- If successful, this could help anesthesiologists use lower, more precise doses of sugammadex to quickly reverse muscle relaxation when the usual drug doesn't work well enough.
- What could go wrong
- This is a small, early-phase trial with only 46 participants, so results may not apply to all patients. Lower doses might not work as well as the standard dose.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
46 people
The number who actually took part.
- Started
-
Jul 2023
- Finished
-
Aug 2024
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients aged 18 years and above who will undergo an elective surgery in the main operating room or outpatient surgery center at Grady Memorial Hospital * Receive general anesthesia (standardized to sevoflurane for maintenance) * Receive rocuronium for NMB * Receive neostigmine for NMB reversal * Achieve a TOF count of at least 3 twitches but not a TOF ratio of 0.9 fifteen minutes after neostigmine has been given * Able and willing to provide informed consent. Exclusion Criteria: * Pregnancy and/or lactating * BMI ≥ 40 * Severe renal impairment, i.e. chronic kidney disease stages IV and V as defined by GFR \< 30 ml/min/1.73 m2 * Severe hepatic impairment, i.e. Child-Pugh score C * Pre-existing neuromuscular disease * Anticipated need for postoperative intubation, and/or known hypersensitivity reactions to rocuronium, neostigmine and/or sugammadex. * Adults unable to consent * Prisoners * Cognitively impaired or Individuals with Impaired Decision-Making Capacity * Individuals who are not able to clearly understand English
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Grady Memorial Hospital
Atlanta, Georgia, 30303, United States
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