A Study To Compare Two Drugs Namely CARBETOCIN VS OXYTOCIN To Prevent Postpartum Hemorrhage
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated deliveryHealth Condition 2: O679- Intrapartum hemorrhage, unspecified
- Registration Number
- CTRI/2022/08/044673
- Lead Sponsor
- MAX SMART SUPERSPECIALITY HOSPITA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria :
1. Study will include pregnant women having vaginal delivery in our hospital .
2. Patient willing to be part of study.
3. Known singleton pregnancy .
Exclusion criteria :
1. Patient who undergo caesarean section .
2. Patient not willing to be include in study ââ?¬â?? not giving consents.
3. Multiple pregnancies.
4. Patient having diabetes mellitus , IHCP,blood disorder ,hypertension ,or on any anticoagulant
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the efficacy of two oxytocics , namely carbetocin and oxytocin in active management of third stage of labor . <br/ ><br>we will give give oxytocic immediately following delivery of anterior shoulder of baby . <br/ ><br> we will see which oxytocics is more efficient , in term of onset of action , duration of action , preventention of PPH. <br/ ><br>Timepoint: we will give give oxytocic immediately following delivery of anterior shoulder of baby in normal vaginal delivery . <br/ ><br> <br/ ><br> we will see which oxytocics is more efficient , in term of onset of action , duration of action , preventention of PPH, amount of blood loss in normal vaginal delivery, . <br/ ><br>we will check all parameter with in 24 hour of delivery. <br/ ><br> <br/ ><br>
- Secondary Outcome Measures
Name Time Method To find out amount of blood loss in each group at the time of normal vaginal delivery . <br/ ><br>To find out change in hematocrit in each group (haemoglobin in third trimester and 24 hour after delivery ) <br/ ><br> To see the side effect in each group with in 24 hour <br/ ><br>To find out the requirement of a second dose of another oxytocics in each groups. <br/ ><br>Timepoint: To find out amount of blood loss in each group at the time of normal vaginal delivery . <br/ ><br>To find out change in hematocrit in each group (haemoglobin in third trimester and 24 hour after delivery ) <br/ ><br>To see the side effect in each group with in 24 hour <br/ ><br>To find out the requirement of a second dose of another oxytocics in each groups (during delivery ). <br/ ><br>
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.