The purpose of this study is to is to determine the clinical effectiveness of a single dose of intravenous (IV) medication for the prevention of labor arrest and cesarean delivery in primiparous women undergoing trial of labor.
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Number of participants that achieve complete dilation of cervix (10cm)
Timeframe: from start of treatment upto 4 hours
Number of participants that achieve complete dilation of cervix (10cm)
Timeframe: from start of treatment upto 6 hours