Placenta Previa Clinical Trial
Official title:
Tranexamic Acid Use in Elective Cesarean Section for Women With Placenta Previa: A Randomized Controlled Trial
Verified date | February 2017 |
Source | Ain Shams University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Tranexamic Acid Use in Elective Cesarean Section for Women With Placenta Previa
Status | Completed |
Enrollment | 86 |
Est. completion date | December 2016 |
Est. primary completion date | November 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Term pregnancy (more than 37 weeks of gestation) - Diagnosis of placenta previa was confirmed by ultrasound - The patient hemoglobin percentage is more than 10 mg/dl Exclusion Criteria: - Invading placenta previa diagnosis was confirmed by Doppler ultrasound studies - Emergency lower segment cesarean section - Associated medical comorbidities |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Ain Shams University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | intra operative blood loss in ml | Calculation of blood loss during cesarean section in the two groups to detect efficacy of Tranexamic acid in reducing blood loss | intraoperative during cesarean section |
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