A clinical trial to study the efficacy of the drug misoprostol administered rectally in reducing excessive bleeding after normal delivery
Not Applicable
- Conditions
- Health Condition 1: null- Women with singleton pregnancy undergoing normal vaginal delivery
- Registration Number
- CTRI/2014/08/004910
- Lead Sponsor
- DrSMCSIMedical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 320
Inclusion Criteria
women with singleton pregnancy
cephalic presentation
>28 weeks of gestational age
Hb >10gms
Exclusion Criteria
patients undergoing cesarean section and instrumental delivery
malpresentation
multiple pregnancy
past history of post partum haemorrhage
coagulopathies
heart disease/renal disease
placenta previa/abruptio placenta
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method fall in haemoglobin and PCV levelsTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method Duration of third stage of labour <br/ ><br>Timepoint: 1 hour