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Oxytocin versus Tranexamic acid and Ethamsylate

Comparative Study Between Oxytocin Versus Tranexamic Acid &Ethamsylate to Reduce Blood Loss Intraoperative and Postoperative During Elective Cesarean Delivery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202101794541918
Enrollment
230
Registered
2021-01-21
Start date
2020-04-01
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

blood loss

Interventions

Tranexamic Acid and Ethamsylate Group

Sponsors

Sayed Galal
Lead Sponsor
Shoubra General Hospital
Collaborator

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1-Pregnant females admitted for elective Cesarean Section 2-Gestational age (38 to 41 weeks) 3- Age of the participants: 20y to 40 years 4- Body Mass Index (18.5 - 29.9) 5-Singleton living fetus. 6-No medical disorders.

Exclusion criteria

Exclusion criteria: 1 - Medical and surgical disorders as thyroid dysfunction, which was excluded by routine thyroid function test (free T3, free T4, and thyroid-stimulating hormone(TSH), all of them should be within normal limits). 2 -Bleeding tendency, was excluded by platelet count, coagulation time, bleeding time, prothrombin time, partial thromboplastin time, and thrombin time (all should be within normal). 3 -Acute and chronic liver or kidney diseases; blood disorders, such as anemia. 4 -Allergy to Tranexamic acid or any drug used. 5 -Risk factors for PPH, such as polyhydramnios, fetal macrosomia, antepartum hemorrhage. 6 - Abnormal placentae such as placenta previa and placental abruption. 7 -Pregnancy complications such as severe pre-eclampsia, Gestational HTN, Gestational DM, and multi Fetal pregnancies, those requiring blood transfusion. 8 - Patients who refused spinal anesthesia.

Design outcomes

Primary

MeasureTime frame
Outcome of the study will be measured in terms of assessment of Hemoglobin level and Hematocrit level pre and post operatively.

Secondary

MeasureTime frame
Outcome of the study will be measured in terms of assessment of Hemoglobin level and Hematocrit level post operatively.

Countries

Egypt

Contacts

Public ContactElsayed ElDesouky

AlAzhar Faculty of medicine

elsayedeldesouky@yahoo.com+201092934978

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Feb 4, 2026