Skip to content

Efficacy of tranexamic acid in reducing blood loss in patients with placenta accrete spectrum

Efficacy of tranexamic acid in reducing blood loss and intra and postoperative complications in patients with placenta accrete spectrum

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201003048909N1
Enrollment
23
Registered
2020-10-26
Start date
2020-10-01
Completion date
Unknown
Last updated
2021-08-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Placenta accrete spectrum. Placenta accreta

Interventions

Intervention 1: Intervention group: Patients in this group will receive 1 gram of intravenous tranexamic acid brand TRANEXIP® made by Caspian Tamin Pharmaceutical Company during 10 minutes immediately

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age over 18 years Diagnosis of placenta accrete spectrum syndrome on ultrasound Singleton pregnancy Cesarean section or cesarean section hysterectomy Patient consent to participate in the study

Exclusion criteria

Exclusion criteria: History of cardiovascular diseases including coronary artery disease, myocardial infarction, severe arrhythmias, and congestive heart failure history of the bleeding disorder including antiphospholipid syndrome (APS) liver and kidney disease known coagulation disorders anemia preoperatively (hemoglobin level < 8 mg/dl) history of preeclampsia or eclampsia in the current pregnancy contraindication to TXA use (history of TXA allergy, venous thromboembolism, active thrombolytic diseases, acquired color vision disorders, history of seizure, pre-known hematuria, and renal failure

Design outcomes

Primary

MeasureTime frame
Amount of estimated blood loss (EBL). Timepoint: Before and after surgery. Method of measurement: CC blood lost.;Complications during and after delivery. Timepoint: Evaluating the patient during and after delivery. Method of measurement: Incidence of complications during and after delivery such as rupture of the bowel, need for hysterectomy, hypogastric ligation, need for laparotomy, and rupture of the bladder.

Secondary

MeasureTime frame
Need to blood products transfusion. Timepoint: during the surgery and the first 24 h after delivery. Method of measurement: Amount of received PRBCs, amount of received platelets, and amount of received FFP.;Duration of hospitalization. Timepoint: Number of hospitalization days after delivery. Method of measurement: Number of hospitalization days.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKobra Shojaei

Ahvaz University of Medical Sciences

amir_fattah2000@yahoo.com+98 61 3292 3985

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 14, 2026