Atosiban in Single Blastocyst Transfer in Patients With Previous Pregnancy Failure and Abnormal Uterine Contractions

NANot yet recruitingINTERVENTIONAL
Enrollment

792

Participants

Timeline

Start Date

October 1, 2025

Primary Completion Date

June 30, 2027

Study Completion Date

September 30, 2027

Conditions
Infertility
Interventions
DRUG

Atosiban

Participants in the atosiban group will receive an intravenous bolus injection of atosiban (37.5 mg/5 mL, , Tractocile®,Ferring Pharma,Geneva, Switzerland) at a rate of 6.75 mg/0.9 mL 30 minutes prior to embryo transfer, followed by a 1-hour intravenous infusion at a rate of 18 mg/h. After 1 hour, the atosiban infusion rate will be reduced to 6 mg/h, with a total dose of 37.5 mg.

DRUG

Placebo Control

Participants in the placebo group will receive an identical saline infusion over the same timeframe. Specifically, saline will be administered intravenously 30 minutes prior to embryo transfer (ET), followed by a continuous intravenous infusion for one hour. This will be succeeded by a further continuous intravenous infusion of saline for 2.125 hours.

Trial Locations (1)

710003

Center for Reproductive Medicine, Northwest Women's and Children's Hospital, Xi'an

All Listed Sponsors
lead

Northwest Women's and Children's Hospital, Xi'an, Shaanxi

OTHER

NCT07185230 - Atosiban in Single Blastocyst Transfer in Patients With Previous Pregnancy Failure and Abnormal Uterine Contractions | Biotech Hunter | Biotech Hunter