a prospective, double-blind, fully randomized controlled, non-inferiority clinical trial to investigate the use of total intravenous anesthesia in pediatric laparoscopic surgery.
Ciprofol is a better alternative to surgical sedatives. The clinical application basis of Ciprofol in pediatric anesthesia is still lacking. Therefore, the investigators designed a prospective, double-blind, fully randomized controlled, non-inferiority clinical trial to investigate the use of all-through intravenous anesthesia in pediatric laparoscopic surgery. Our main hypothesis is that in pediatric surgery, using Ciprofol by intravenous anesthesia, the extubation time is no longer than that the propofol group.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
86
Tongji hospital
Wuhan, Hubei, China
Extubation time
Time interval between drug withdrawal and removal of the tracheal catheter
Time frame: up to 1 hour
Aldrete Score
In the PACU, Investigators using Aldrete score scale(0- 10 points)
Time frame: up to 2 hours
Emergence Agitation
In the PACU, Investigators assessed emergence delirium using PAED 0-20 points)
Time frame: up to 2 hours
Postoperative Pain
use the FLACC pain score(0- 10 points)
Time frame: 24 hours
Postoperative nausea and vomiting
Investigators assessed postoperative nausea and vomiting BARF scale(0-10points)
Time frame: 24 hours
satisfaction degree
Child and/or Parent Satisfaction Survey (0-10 points)
Time frame: 24 hours
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