A comparison between two regimes for Labour induction in Intrauterine fetal death
- Conditions
- Health Condition 1: null- WOMEN diagnosed with intrauterine foetal death after 20 weeks of pregnancy.
- Registration Number
- CTRI/2014/03/004489
- Lead Sponsor
- RS MEDICAL COLLEGE KOLKATA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 100
Women with period of gestation >20 weeks presenting with dead fetus as confirmed by ultrasonography without clinical evidence of active labour, bleeding per vagina, or ruptured membranes were included.
Women who had known allergy to mifepristone and misoprostol or had contraindications for the use of two drugs were excluded.
b. Women with known previous transmural uterine incision (caeserian section, myomectomy), with grand multiparity ( > 4 ,with Haemoglobin level below 8 gm/dl or with any medical problem as renal, liver, cardiovascular diseases or coagulopathy were also excluded.
c. Women who had low lying placenta as demonstrated by ultrasonography and who showed evidence of infection, who were in active labour or had bleeding or leaking per vagina were not included.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method .Rate of successful delivery without additional intervention. <br/ ><br>2. Induction to delivery intervalTimepoint: 24 hours <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1.additional interventions needed <br/ ><br>2.side effects and complications. <br/ ><br>Timepoint: 1.24 hours <br/ ><br>2.6 weeks