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Concurrent Oxytocin With Membrane Sweeping Versus Dinoprostone Pessary in Labor Induction of Multiparous Women at Term

Plain-language guide to NCT02618096: not phased randomized trial of Oxytocin, 154 participants. Who took part, design and what was measured.

Key Facts

Registry ID
NCT02618096
Phase
not phased
Status
completed
Start
2015-10
Completion (planned or actual)
2018-10
Participants
154 (actual)
Design
randomized, open label (everyone knows who gets what), treatment
Conditions studied
Failed Induction of Labor
Results posted
not yet

What This Study Did, in Plain Language

What Was Tested

This registered not phased trial tested Oxytocin.

The purpose of this study is to compare concurrent oxytocin with membrane sweeping versus dinoprostone pessary in labor induction for multiparas at term with an unfavorable cervix.

It had two arms (groups): Oxytocin & Membrane sweeping (active comparator) and Oxytocin & Dinoprostone (active comparator).

Women assigned to "Concurrent oxytocin with membrane sweeping" had their cervix swept by inserting the examining finger as high as possible past the internal cervical os, followed by oxytocin infusion the next day.

The registry classes the interventions as drug and procedure.

Who Took Part

The registry lists 154 actual participants took part.

It was open to women only.

Healthy volunteers were not accepted; participants needed the condition being studied.

Examples of who could join: Gestational age \>=37.0 weeks. Bishop score \<=6. Intact amniotic membrane. Absence of labor. Live fetus with vertex presentation.

The full record lists 8 inclusion and 2 exclusion criteria; among the exclusions: multiple pregnancy; placenta previa.

How the Study Was Run

The set-up was randomized, parallel-group and open-label.

Random assignment meant chance, not the researchers, decided who got Oxytocin and who got the comparison, which limits bias.

Groups ran in parallel: each of the participants stayed in one arm throughout.

Being open-label, the Oxytocin study did not mask who received what.

It started in 2015-10 with completion listed for 2018-10.

It ran at 1 site in South Korea.

Its stated primary purpose is treatment.

What Was Measured

Primary outcome: Vaginal delivery within 24 hours.

It also tracked 3 secondary outcomes, for example Successful labor induction, Incidence of cesarean delivery and The interval from start of oxytocin to delivery.

What This Means in Plain Language

Put simply, this is a not phased, randomized trial of Oxytocin in 154 people.

The trial is marked completed; no results are posted to the registry yet, so nothing here describes outcomes.

More context: the Oxytocin compound page, all human trials.

Our Notes on the Compound

Oxytocin: A peptide hormone with established obstetric medical uses and a less settled role in research on behavior, sexual function and appetite.

Related Pages

Source: ClinicalTrials.gov record. This explanation is written by PeptideWhiz from the public record. For research and education only. Not medical advice; no dosing information is given.