CTRI/2014/03/004491Recruiting未知
Efficacy and safety of 400 microgram misoprostol by sublingual route to augment routine management of third stage of labour in high risk women following vaginal delivery.
RS MEDICAL COLLEGE KOLKATA0 sites200 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- 未知
- Status
- Recruiting
- Sponsor
- Enrollment
- 200
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •Women with one or more of the high risk factors as
- •multiple pregnancy
- •polyhydramnios
- •prolonged labour
- •labor augmented by oxytocin.
- •H/O PPH in previous pregnancy.
- •Post caesarean section (for vaginal delivery)
- •Obese patient (BMJ >30)
- •Grand multipara
- •Severe preeclampsia/eclampsia.
- •Anaemia(hb <10gm%)
Exclusion Criteria
- •Any contraindications for the use of misoprostol and oxytocin such as known hypersensitivity, asthma, epilepsy etc.
- •Cardiovascular, hepatic, haematological disorders.
- •Temperature >38ï?°C
Investigators
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