A Clinical Trial Evaluating the Efficacy and Safety of HSK21542 in PONV

NACompletedINTERVENTIONAL
Enrollment

200

Participants

Timeline

Start Date

November 10, 2023

Primary Completion Date

February 28, 2024

Study Completion Date

May 15, 2024

Conditions
Postoperative Nausea and Vomiting
Interventions
DRUG

HSK21542-60μg

HSK21542 injection of 60 μg was administered once within 15 min before the end of surgery, and was administered by intravenous bolus injection for no less than 30 s;

DRUG

HSK21542-120μg

HSK21542 injection of 120 μg was administered once within 15 min before the end of surgery, and was administered by intravenous bolus injection for no less than 30 s;

DRUG

HSK21542-180μg

HSK21542 injection of 180 μg was administered once within 15 min before the end of surgery, and was administered by intravenous bolus injection for no less than 30 s;

DRUG

Placebo

A placebo was administered once within 15 min before the end of surgery, and was administered by intravenous bolus injection for no less than 30 s;

Trial Locations (1)

Unknown

Sichuan Provincial People's Hospital, Sichuan

All Listed Sponsors
lead

Sichuan Provincial People's Hospital

OTHER

NCT06170476 - A Clinical Trial Evaluating the Efficacy and Safety of HSK21542 in PONV | Biotech Hunter | Biotech Hunter