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Efficacy of Preoperative Intravenous Tranexamic Acid Before Caesarean Section in Placenta Previa

Phase 2
Completed
Conditions
intraoperative blood loss in pregnant woman undergoes caesarean section due to placenta previa
Keyword: Tranexamic acid, preoperative, placenta previa, intraoperative blood loss, caesarean section
Registration Number
TCTR20220930003
Lead Sponsor
none
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Female
Target Recruitment
60
Inclusion Criteria

1. All pregnant woman with placenta previa diagnosed by transabdominal or transvaginal ultrasound(if not clearly by TAS) confirmed at GA 28 week by obstetricians
3.undergoing caesarean delivery for placenta previa include elective c/s at term (37+ week) or emergency c/s due to placenta previa
4.Repeat ultrasound confirm before caesarean section
5.Age > 18 year and already informed consent

Exclusion Criteria

1. Allergic patient to transamine
2. Undergo caesarean section due to placenta previa before GA 28 week
3. follow up by ultrasound during antenatal care and diagnosis was changed
4. Patient with showed any sign of adherent placenta on ultrasound
5. Patient with active cardiac, hepatic, renal disease
6. patient with risk factor for VTE such as prior VTE, thrombophilia disease**, hematologic cancer, immobilize patient, first degree relative history of VTE, morbid obesity BMI>40
7.Underlying disease of Coagulopathy, thrombocytopenia or on anticoagulant
8. patient cannot make decision

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
intraoperative blood loss intraoperative intraoperative blood loss measured by amount of blood in suction add with diffrent weight between soaked gauze and dry gauze
Secondary Outcome Measures
NameTimeMethod
incidence of PPH 24 hour postpartum measured blood loss 24 hr postpartum more than 1000 ml
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