Perioperative Use of Atosiban for Ultrasound-indicated Cerclage to Reduce Spontaneous Preterm Birth(sPTB)

NACompletedINTERVENTIONAL
Enrollment

334

Participants

Timeline

Start Date

January 3, 2018

Primary Completion Date

February 12, 2024

Study Completion Date

April 12, 2024

Conditions
Cervical CerclagePremature Birth
Interventions
DRUG

Atosiban

Women in the atosiban group received i.v. atosiban (Manufacturer: Pfizer, Germany) 30 min before the surgery with a bolus dose of 6.75 mg, and the infusion was continued with an infusion rate of 18 mg/h for 3 h. The dose of atosiban was then reduced to 6 mg/h for another 45 h.

DRUG

Normal saline

Participants in the placebo group received only normal saline infusion for the same duration as atosiban group.

Trial Locations (2)

400000

The First Affiliated Hospital of Chongqing Medical University, Chongqing

400016

Women and Children's Hospital of Chongqing Medical University, Chongqing

All Listed Sponsors
collaborator

First Affiliated Hospital of Chongqing Medical University

OTHER

lead

Children's Hospital of Chongqing Medical University

OTHER

NCT06537778 - Perioperative Use of Atosiban for Ultrasound-indicated Cerclage to Reduce Spontaneous Preterm Birth(sPTB) | Biotech Hunter | Biotech Hunter