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Oral misoprostol solution in comparison to vaginal misoprostol for induction of labour in a randomized controlled trial
Article | IMSEAR | ID: sea-207983
ABSTRACT

Background:

With more than 15% of all gravid women requiring prostaglandins in cervical ripening and labour induction. However, evidence is not clear about the preferred route or dose of the drug. So, this study was designed with objectives to compare the induction delivery interval and safety of titrated oral misoprostol solution with vaginal misoprostol for labour induction in term primigravida women.

Methods:

This randomized controlled clinical trial was conducted on a total of 100 patients randomly selected among primigravida at term women undergoing induction of labour for obstetric or medical indication for labour induction in Ain Shams University Maternity Hospital. They were divided into two Groups Group I patients undergoing induction of labour using misoprostol oral solution and Group II patients undergoing induction of labour using vaginal misoprostol.

Results:

Oral misoprostol solution has less induction delivery duration and less side effects than vaginal misoprostol. The induction-delivery time with the oral route compared to the vaginal one (15.2 versus 20.3 hours respectively) with significant p-value (<0.001).

Conclusions:

Titrated oral misoprostol is safe and effective for labour induction in primigravida patients with unfavorable cervix.

Full text: Available Index: IMSEAR (South-East Asia) Type of study: Controlled clinical trial Year: 2020 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Type of study: Controlled clinical trial Year: 2020 Type: Article