Induction of labour in pregnancy with intrauterine fetal demise
Not Applicable
- Registration Number
- CTRI/2022/10/046254
- Lead Sponsor
- dr Sanjay Prabhasbhai Parmar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All ANC mothers with gestational ages of greter than 24 weeks with IUFD pregnancy who were willing to give written informed consent will be recruited in this study from the labour room.
Exclusion Criteria
less than 24 weeks of pregnancy
-hypersensitivity to prostaglandins.
-Medical condition like severe anaemia, adrenal failure, liver disease, hypertension, bronchial asthma, heart disease.
- scarred uterus
- grand multipara.
- Ruptured membrane
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To measure Induction-Delivery interval and to compare between both groups.Timepoint: From induction time to delivery time
- Secondary Outcome Measures
Name Time Method To measure Frequency of side effect (nausea, vomiting, diarrhoea, pain). <br/ ><br>To measure total dose of induction agent used. <br/ ><br>Timepoint: From Induction time to delivery time