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Induction of Labor in Term Pregnancies With Unfavourable Cervix — RAND  

Induction of Labor Affected Fetus / Newborn Clinical Trial

Official title:
Comparison of Intracervical and Intravaginal Application of Prostaglandin E2 for Induction of Labour in Term Pregnancies With Unfavourable Cervix

Clinical Trial Summary

This is a prospective randomized trial comparing two prostaglandin E2 (dinoprostone) agents used for labor induction in pregnant women with term pregnancies and unfavorable cervix.

Clinical Trial Description

This prospective randomized trial includes pregnant women with term pregnancies, indication for labor induction and an unfavorable cervix. These women are randomized into two groups: one group is induced using an intracervical prostaglandin E2 (PGE2, dinoprostone) formulation, the other using an intravaginal PGE2 formulation. Main outcome is time period between beginning of labor induction to delivery, and a reduction of four hours is considered clinically significant. ;

Study Design

Related Conditions & MeSH terms

  • Induction of Labor Affected Fetus / Newborn
  • Prostaglandins Causing Adverse Effects in Therapeutic Use
Clinical Trial Details
NCT number NCT04280874
Study type Interventional
Source Clinical Hospital Merkur
Contact
Status Completed
Phase Phase 4
Start date December 10, 2018
Completion date July 1, 2020
View Details
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