Experience with Atosiba
Not Applicable
Completed
- Conditions
- Health Condition 1: O600- Preterm labor without delivery
- Registration Number
- CTRI/2019/01/017054
- Lead Sponsor
- Army Research and Referral Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 150
Inclusion Criteria
All patients with preterm labour Singleton/ multi fetal gestation beyond 24weeks of gestation to
33 weeks + 6 days with intact amniotic membranes
Exclusion Criteria
1. All patients with preterm rupture of membranes
2. All patients of abruptio placenta
3. All patients less than 24 weeks of gestation
4. All patients more than 34 weeks of gestation
5. All patients with fever , tachycardia and positive CRP in maternal blood on admission
6. All patients with IUD /congenital anomaly
7. Patients needing more than one tocolytic agent.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Proportion of patients who will be undelivered upto 72 hours after completion of treatment phase and those not delivered till the end of 7 daysTimepoint: Throughout study duration
- Secondary Outcome Measures
Name Time Method 1.Perinatal death. <br/ ><br>2.Mode of delivery. <br/ ><br>3.Emergency caesarean (if any) <br/ ><br>Timepoint: At the time of delivery