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Comparison extra amniotic salin infusion and vaginal isoniazide for cervical ripening before induction and labour duration in term and post term pregnancy

Phase 1
Conditions
Pregnancy.
Normal pregnancy
Registration Number
IRCT2015040721506N2
Lead Sponsor
Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
150
Inclusion Criteria

1- single tone pregnancy 2- bishop score<5.
Exclusion criteria: 1-macrosomia EFW> 5 Kg. 2- not reassuring NST. 3- PROM 4-AFI<5 Cm. 5- history of kidney and liver diseases. 6-history of Cesarian section. 7- low lying placenta. 8- any contraindication of isoniazide such as vomiting, nausea, visual defect, vertigo. 9- no cephalic presentation. 10- unexplained vaginal bleeding. 11- labor phase. 12- organic disease. 12- grand multiparity

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Bishap score. Timepoint: Before intervetion and before induction. Method of measurement: Clinical examination.
Secondary Outcome Measures
NameTimeMethod
Interval intervention until active phase. Timepoint: Start of intervention till delivery. Method of measurement: Minutes.;Interval between intervention till labour. Timepoint: Start of intervention till delivery. Method of measurement: Minutes.;Time intrval between intervetion till indoction of labour. Timepoint: start of intervention. Method of measurement: minute.;Compliation vomating and nausia and icter and vertigo. Timepoint: Start of intervention till delivery. Method of measurement: Examination and question.
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