ntroduction: Cervical ripening methods are always used to prepare cervix during labor induction. The aim of this study was to compare the effects of oxytocin alone and oxytocin in combination with intravenous and oral propranolol on labor progression in natural childbirth. Materials and Methods: This clinical trial study was conducted on 120 pregnant women with 38-41 weeks of gestational age. They divided into three groups using triplex random blocks. The sample size in each group was 40 cases. The Induction of labor started for the first group using oxytocin alone, the second group received oxytocin in combination with intravenous propranolol and the third group received oxytocin along with oral propranolol. The duration of first and secon...
Background: Most common cause for delay in labor is due to inefficient uterine contractions. Various...
Abstract Objectives: To compare the safety and efficacy of prostaglandin E2 gel with I.V. oxytocin...
A double-blind randomised trial was conducted on women with gestational age of 40�42 weeks of preg...
BACKGROUND: Prolonged labor can lead to maternal and neonatal complications. The purpose of this stu...
CONTEXT: Misoprostol, a synthetic E1 methyl analog prostaglandin, is at present receiving attention ...
Abstract- Labor induction despite an unriped cervix is one of the most common indications of the use...
OBJECTIVES: To investigate the efficacy of two labor induction protocols. STUDY DESIGN: In this retr...
Objective: To compare the effects of oxytocin and amniotomy or vaginal prostaglandin E2 (PGE2) for i...
Objective: To compare the effects of oxytocin and amniotomy or vaginal prostaglandin E-2 (PGE(2)) fo...
Objective: To compare the effects of oxytocin and amniotomy or vaginal prostaglandin E-2 (PGE(2)) fo...
Abstract- The purpose of this study was to compare the efficacy and safety of misoprostol and oxytoc...
To compare the effects of oxytocin and amniotomy or vaginal prostaglandin E2 (PGE2) for induction of...
Background: To compare oral misoprostol with intravenous oxytocin for labour augmentation in nullipa...
A randomized clinical trial study was undertaken to evaluate the effect of intravenous oxytoxin (50 ...
OBJECTIVES: The aim of this study is to compare the safety and efficacy of titrated oral with vagin...
Background: Most common cause for delay in labor is due to inefficient uterine contractions. Various...
Abstract Objectives: To compare the safety and efficacy of prostaglandin E2 gel with I.V. oxytocin...
A double-blind randomised trial was conducted on women with gestational age of 40�42 weeks of preg...
BACKGROUND: Prolonged labor can lead to maternal and neonatal complications. The purpose of this stu...
CONTEXT: Misoprostol, a synthetic E1 methyl analog prostaglandin, is at present receiving attention ...
Abstract- Labor induction despite an unriped cervix is one of the most common indications of the use...
OBJECTIVES: To investigate the efficacy of two labor induction protocols. STUDY DESIGN: In this retr...
Objective: To compare the effects of oxytocin and amniotomy or vaginal prostaglandin E2 (PGE2) for i...
Objective: To compare the effects of oxytocin and amniotomy or vaginal prostaglandin E-2 (PGE(2)) fo...
Objective: To compare the effects of oxytocin and amniotomy or vaginal prostaglandin E-2 (PGE(2)) fo...
Abstract- The purpose of this study was to compare the efficacy and safety of misoprostol and oxytoc...
To compare the effects of oxytocin and amniotomy or vaginal prostaglandin E2 (PGE2) for induction of...
Background: To compare oral misoprostol with intravenous oxytocin for labour augmentation in nullipa...
A randomized clinical trial study was undertaken to evaluate the effect of intravenous oxytoxin (50 ...
OBJECTIVES: The aim of this study is to compare the safety and efficacy of titrated oral with vagin...
Background: Most common cause for delay in labor is due to inefficient uterine contractions. Various...
Abstract Objectives: To compare the safety and efficacy of prostaglandin E2 gel with I.V. oxytocin...
A double-blind randomised trial was conducted on women with gestational age of 40�42 weeks of preg...