Overview
Tranexamic Acid and Ethamsylate For Preventing PPH in Patient Undergoing LSCS at High Risk For PPH
Status:
Unknown status
Unknown status
Trial end date:
2016-07-01
2016-07-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
The aim of this study is to compare the effect of low dose of Tranexamic acid (1gm) and Ethamsylate (1gm) after prophylactic oxytocin administration versus placebo with prophylactic oxytocin given in the 2 minutes after child delivery in patient undergoing LSCS at high risk for post partum hemorrhagePhase:
Phase 1/Phase 2Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Ahmed AlanwarTreatments:
Ethamsylate
Tranexamic Acid
Criteria
Inclusion Criteria:1. Women undergoing elective caesarean section
2. Patient having one or more risk factor for PPH
- Multiple pregnancy
- Polyhydramnios (AFI >25cm)
- Macrocosmic baby (>4.5 Kg)
- Prolonged , augmented and obstructed labour
- Obese patients(BMI >30)
- Premature rapture of membranes
- Previous history of PPH
3. Age ≥18 years
4. Gestational Age ≥ 35 Weeks
5. Informed Oral Consent From The Patient
Exclusion Criteria:
1. History of venous thrombosis (DVT and/or Pulmonary embolism) OR arterial thrombosis
(angina pectoris , myocardial infarction, stroke)
2. History of epilepsy or seizure
3. Any Known Cardiovascular , renal or liver Disease
4. Autoimmune Diseases
5. Sickle Cell Disease
6. Severe hemorrhagic Disease
7. Placenta Previa.
8. Morbidly adherent Placenta
9. Abruptio placenta
10. Eclampsia, hemolysis, elevated liver enzymes, and low platelet count syndrome
11. Administration Of low molecular weight heparin or Anti platelets the week before
delivery .