Background: The comparison of same,equal and low dose of misoprostol by the oral and vaginal routes for induction of labour at term requires further elucidation.Objective: To compare the efficacy and safety of 25 micrograms (ug) of oral misoprostol with 25ug vaginal misoprostol for induction of labor at term.Methods: A randomised control trial that involved 169 consented women with indication for induction of labor. A total of 85 women had oral misoprostol while 84 women had vaginal misoprostol. The oral misoprostol dose (25ug) was repeated every 2 hours, while the vaginal dose (25ug) was repeated every 6 hours for a maximum duration of 24 hours or when need arose for intervention. Data was analysed using SPSS version 20.Results: The mean i...
Background: It was a randomized controlled prospective study. A large number of women in their advan...
Objective: The main goal of the following study is to observe the contrast between the efficacy of t...
A double-blind randomised trial was conducted on women with gestational age of 40�42 weeks of preg...
Background: To compare the efficacy and safety of oral versus vaginal administration of Misoprostol ...
Background: To compare the Induction – Deliveryinterval between Oral and Vaginal route of Misoprosto...
Background: Induction of labor for postdate pregnancy using misoprostol is one of the most common in...
OBJECTIVES: The aim of this study is to compare the safety and efficacy of titrated oral with vagin...
Objective: To compare the outcome of oral misoprostol (20µg 2 hourly) with vaginal misoprostol (25µg...
Objective. To compare the efficacy of vaginal misoprostol (25 μg) to oral misoprostol (100 μg) in la...
Background/Aim: Labor is induced in 1 out of 5 pregnancies. This is why we aimed to compare two diff...
OBJECTIVE: To compare the efficacy of similar buccal and vaginal misoprostol doses for induction of ...
To compare the efficacy and safety of two misoprostol dosing regimens for induction of labour in pri...
Background: The aims of this randomised, double blind, placebo controlled trial were to compare vagi...
Objective: To compare the efficacy of 100 μg of oral misoprostol with 3 mg prostaglandin E2 vaginal...
Objective: To compare the efficacy and safety of a single dose of 50 µg oral misoprostol with 25 µg ...
Background: It was a randomized controlled prospective study. A large number of women in their advan...
Objective: The main goal of the following study is to observe the contrast between the efficacy of t...
A double-blind randomised trial was conducted on women with gestational age of 40�42 weeks of preg...
Background: To compare the efficacy and safety of oral versus vaginal administration of Misoprostol ...
Background: To compare the Induction – Deliveryinterval between Oral and Vaginal route of Misoprosto...
Background: Induction of labor for postdate pregnancy using misoprostol is one of the most common in...
OBJECTIVES: The aim of this study is to compare the safety and efficacy of titrated oral with vagin...
Objective: To compare the outcome of oral misoprostol (20µg 2 hourly) with vaginal misoprostol (25µg...
Objective. To compare the efficacy of vaginal misoprostol (25 μg) to oral misoprostol (100 μg) in la...
Background/Aim: Labor is induced in 1 out of 5 pregnancies. This is why we aimed to compare two diff...
OBJECTIVE: To compare the efficacy of similar buccal and vaginal misoprostol doses for induction of ...
To compare the efficacy and safety of two misoprostol dosing regimens for induction of labour in pri...
Background: The aims of this randomised, double blind, placebo controlled trial were to compare vagi...
Objective: To compare the efficacy of 100 μg of oral misoprostol with 3 mg prostaglandin E2 vaginal...
Objective: To compare the efficacy and safety of a single dose of 50 µg oral misoprostol with 25 µg ...
Background: It was a randomized controlled prospective study. A large number of women in their advan...
Objective: The main goal of the following study is to observe the contrast between the efficacy of t...
A double-blind randomised trial was conducted on women with gestational age of 40�42 weeks of preg...