Induction of Labor Affected Fetus / Newborn Clinical Trial
Official title:
Nitric Oxide Donor Isosorbide Mono Nitrate for Cervical Ripening in Induction of Labor
The study aims to evaluate and assess the effectiveness and safety of vaginal administration of isosorbide mono nitrate (ISMN) to induce cervical ripening and shorten the interval time between induction and delivery in women undergoing induction of labor. Research Hypothesis: In women undergoing induction of labor, vaginal administration of isosorbide mono nitrate (IMN) is effective to induce cervical ripening and shorten the interval time between induction and delivery. . Research Questions: Does vaginal administration of isosorbide mono nitrate (IMN) induce cervical ripening and shorten the interval time between induction and delivery in women undergoing induction of labor?
Patient and methods Type of study: Prospective double blinded randomized placebo-controlled clinical trial. Study setting: The study will be conducted at Cairo university in labor ward of Kasr El Ainy Hospital. Study period: approximately 6 months from June 2018 to December 2018. Study population: Patients will be recruited in this study those attending labor ward at kasr el ainy hospital for induction of labor after 39 weeks of gestation. ;
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