None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To measure Induction-Delivery interval and to compare between both groups.Timepoint: From induction time to delivery time | — |
Secondary
| Measure | Time frame |
|---|---|
| To measure Frequency of side effect (nausea, vomiting, diarrhoea, pain). To measure total dose of induction agent used. Timepoint: From Induction time to delivery time | — |
Countries
India
Contacts
Baroda Medical College and SSG hospital vadodara