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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03060889
Other study ID # AAbdelaziz
Secondary ID
Status Completed
Phase Phase 3
First received January 10, 2017
Last updated February 21, 2017
Start date February 2016
Est. completion date December 2016

Study information

Verified date February 2017
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Tranexamic Acid Use in Elective Cesarean Section for Women With Placenta Previa


Description:

Tranexamic Acid Use in Elective Cesarean Section for Women With Placenta Previa to detect efficacy of Tranexamic acid in decreasing blood loss


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Tranexamic acid
10 mg/kg body weight will be given with induction of anesthesia by intravenous infusion

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Outcome

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
See also
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Recruiting NCT02590484 - The Cervix as a Natural Tamponade in Postpartum Hemorrhage Caused by Placenta Previa and Placenta Previa Accreta N/A
Recruiting NCT05802251 - Sonographic Parameters and Risk of Antepartum Hemorrhage in Asymptomatic Women With Placenta Previa: A Cohort Study
Completed NCT03542552 - Nifedipine Versus Magnesium Sulfate for Prevention of Preterm Labor in Symptomatic Placenta Previa Phase 3
Recruiting NCT03124472 - Effect of Uterine Artery Ligation Prior to Uterine Incision in Women With Placenta Previa N/A
Recruiting NCT03633175 - Progesterone in Patients With Placenta Previa Phase 2