About this trial
This study aims to compare the use of sugammadex (domestic) and neostigmine for antagonism after thoracic surgery, and observe the effect of sugammadex (domestic) on neuromuscular blockade antagonism after thoracic surgery, in order to provide a basis for optimizing the use of muscle relaxants and their antagonists during anesthesia.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Patients who undergo elective lung surgery under general anesthesia and require endotracheal intubation;
Age>18 years old, gender not limited;
American Society of Anesthesiologists ASA Level I-III;
Use rocuronium bromide for neuromuscular blockade;
Disqualifiers
The patient explicitly refused to participate in this trial;
Family history of malignant hyperthermia, patients with allergies to sodium sulbactam, neostigmine ingredients and their excipients, and patients with allergies to drugs used during general anesthesia;
Patients with tracheal malformations or suspected difficult airways, coagulation dysfunction, severe liver and kidney dysfunction, and severe lung disease;
Patients who are not extubated and sent to the ward or ICU after surgery;
Trial design
Parallel
Treatments tested in this trial
SUGAMMADEX SODIUM 100 Mg in 1 mL
DrugThe dose of Sugammadex Sodium 100 Mg in 1 mL is 2mg/kg
Neostigmine
DrugNeostigmine is 50 μg/kg
Treatment groups
Trial outcomes
Primary outcomes
Muscle relaxation recovery time
The time from using antagonists to TOFr recovery to 0.9
Sponsors and contacts
Click on the lead sponsor to view all of their trials.