Health Condition 1: null- WOMEN WITH ONE OR MORE OF RISK FACTORS FOR PPH UNDERGOING CESAREAN SECTION.
Conditions
Interventions
Intervention1: misoprostol and oxytocin: study group will receive 400microgram of misoprostol sublingually along with oxytocin 10units intramuscular and 10 units in iv drip.
Control Intervention1: pla
Sponsors
NRS MEDICAL COLLEGEKOLKATA
Eligibility
Inclusion criteria
Inclusion criteria: Women undergoing Cesarean section having one or more of the following high risk factors will be enrolled â?? Multiple pregnancy Polyhydramnios foetal macrosomia(more than 4 kg) prolonged / obstructed labor( as per standard guideline after partographic monitoring) H/O PPH in previous delivery Obese patient (BMI >30) Grand multipara APH Anaemic women (Hb less than 10gm/dl.)
Exclusion criteria
Exclusion criteria: Any contraindications for the use of misoprostol and oxytocin such as known hypersensitivity, asthma, epilepsy , Cardiovascular, hepatic, haematological disorder, Temperature >38ï?°C
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. introperative and postoperative blood loss ( 4 hours) . 2. drop of haemoglobin and haematocrit post delivery at 24 hours. Timepoint: 1. introperative and postoperative blood loss ( 4 hours) . 2. drop of haemoglobin and haematocrit post delivery at 24 hours. | — |
Secondary
| Measure | Time frame |
|---|---|
| i) Need for blood transfusion . ii) Need of additional uterotonic . iii) Side effects and complications. Timepoint: 24 HOURS | — |
Countries
India
Contacts
Public ContactDR PICKLU CHAUDHURI
N.R.S MEDICAL COLLEGE,KOLKATA
Outcome results
None listed