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A clinical trial to see the effect of Tranexamic Acid in reducing blood loss during cesarean sectio

Phase 4
Completed
Conditions
Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
Registration Number
CTRI/2021/02/031579
Lead Sponsor
AIIMS Raipur
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
72
Inclusion Criteria

1.Subjects with singleton pregnancy (parity not more than 3)

2.Age � 18 and < 35 years.

3.� 37 weeks and < 42 weeks of gestation

4.Alive fetus.

5.Hb � 9 g % in recent 3rd trimester report.

6.Subjects receiving spinal anaesthesia for Cesarean Section

Exclusion Criteria

1.History of venous (deep vein thrombosis and/or pulmonary embolism) or arterial (angina pectoris, myocardial infarction, stroke) thrombosis

2.Subjects with medical disorders like chronic hypertension, renal disease, heart disease, liver disease complicating pregnancy

3.Known case of coagulation disorders

4.Pregnancy related complication like severe preeclampsia, multiple pregnancy, polyhydramnios, and macrosomia, with abnormal placentation, previous two or more caesarean sections

5.Intrauterine death

6.Woman on anticoagulant therapy during the week before delivery

7.Sickle cell disease

8.History of seizures

9.Allergy to TXA.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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