Postpartum Hemorrhage
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Pregnant women aged >= 18 years; 2. Twin pregnancy confirmed by ultrasound; 3. Gestational age >= 34+0 weeks; 4. Elective cesarean section (non emergency); 5. Preoperative hemoglobin >= 90g/l; 6. ASA class II-III; 7. Sign informed consent.
Exclusion criteria
Exclusion criteria: 1. Known allergy to oxytocin or ergometrine; 2. Contraindications for ergometrine use (such as hypertension, cardiovascular disease, etc.); 3. Placenta previa; Placenta accreta; Suspected placenta accreta; 4. Known coagulation dysfunction or platelet count = 5cm; or multiple fibroids with more than 3 and a single fibroid >= 2cm; 7. Polyhydramnios (amniotic fluid index > 24cm); 8. Macrosomia (estimated weight of any fetus > 4000g); 9. Other operations (such as ovarian cyst removal, uterine fibroids removal, etc.) are required during the operation; 10. Participating in other clinical studies; 11. The researcher believes that it is not suitable to participate in this experiment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of the composite outcome of postpartum hemorrhage and related complications within 24 hours postpartum.; | — |
Secondary
| Measure | Time frame |
|---|---|
| Severe postpartum hemorrhage (>=1000 mL) within 24 hours postpartum.;Proportion of patients requiring additional second?line uterotonics.;The magnitude of hemoglobin decrease at 24 and 48 hours postoperatively.;Cardiovascular adverse events;Quality of postoperative recovery; | — |
Countries
China
Contacts
The First Affiliated Hospital of Chongqing Medical University