A STUDY TO COMPARE THE EFFECT OF TRANEXAMIC ACID ON HYPERTENSIVE WOMEN AFTER DELIVERY BY MEASURING BLOOD LOSS
Not Applicable
- Conditions
- Health Condition 1: I169- Hypertensive crisis, unspecified
- Registration Number
- CTRI/2021/04/032578
- Lead Sponsor
- PRIYANKA UMBARJE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age more than 18 years
Gestational age >28 weeks
All the patients with spontaneous onset of labour
All the hypertensive patients i.e gestational hypertension, pre eclampsia, eclampsia, and chronic hypertension.
Exclusion Criteria
Previous Caesarean section
Multiple pregnancy, polyhyramnios
Placenta previa or placenta accreta syndrome, placental abruption
Instrumental deliveries
Grand multiparity
Chorioamnionitis
Anemia with Hb <7
Induced labour
Women with medical disorders like thromboembolic disease, heart disease, liver, renal disorders, epilepsy, Diabetes mellitus or Gestational diabetes mellitus.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method TO MEASURE THE BLOOD LOSS AFTER GIVING THE INTERVENING DRUGTimepoint: TO MEASURE THE BLOOD LOSS AFTER GIVING THE INTERVENING DRUG WITHIN ONE HOUR. THE SIDE EFFECTS OF DRUG ARE OBSERVED TILL 3 MONTHS
- Secondary Outcome Measures
Name Time Method ATimepoint: NA