Labor Clinical Trial
Official title:
A Comparison of Titrated Oral Misoprostol Solution to Intravenous Oxytocin for Labor Augmentation: A Randomized Controlled Trial
The purpose of this study is to compare the efficacy and safety of titrated oral misoprostol solution with intravenous oxytocin for labor augmentation in women without adequate uterine contractions.
Numerous labor course necessitate augmentation when uterine contractions are inadequate.
When the cervix is favorable, labor augmentation attempts are more likely to be successful.
Augmentation is these women is traditionally undertaken with intravenous oxytocin and
amniotomy, either alone or in combination.
In our previous trial, it has been proven that the method of titrated oral misoprostol is
associated with a lower incidence of uterine hyperstimulation and a lower cesarean delivery
rate than vaginal misoprostol for labor induction in patients with unfavorable cervix.
Because administering Misoprostol solution is easy and cost saving, it is worth to develop
this novel method in labor augmentation.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
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