Clinical Trials Directory

Trials / Unknown

UnknownNCT02902653

Efficacy and Safety of Hourly Titrated Misoprostol Versus Vaginal Dinoprostone and Misoprostol for Cervical Ripening and Labor Induction

Efficacy and Safety of Hourly Titrated Misoprostol Versus Vaginal Dinoprostone and Misoprostol for Cervical Ripening and Labor Induction: Randomized Clinical Trial

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
372 (estimated)
Sponsor
Oihane Lapuente Ocamica · Other Government
Sex
Female
Age
18 Years – 55 Years
Healthy volunteers
Not accepted

Summary

This study evaluates the efficacy and safety of the administration of oral misoprostol versus vaginal dinoprostone and vaginal misoprostol for cervical ripening and labor induction.

Conditions

Interventions

TypeNameDescription
DRUGOral misoprostolhourly titrated misoprostol
DRUGVaginal misoprostolAdministration of 25 microgs every 6 hours, maximum 150 microgr
DRUGVaginal dinoprostoneVaginal delivery system of 10mg of dinoprostone

Timeline

Start date
2016-09-01
Primary completion
2020-09-01
Completion
2020-09-01
First posted
2016-09-16
Last updated
2018-02-12

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT02902653. Inclusion in this directory is not an endorsement.