NCT02618096

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
154

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Oct 2015

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 25, 2015

Completed
6 days until next milestone

Study Start

First participant enrolled

October 1, 2015

Completed
2 months until next milestone

First Posted

Study publicly available on registry

December 1, 2015

Completed
2.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2018

Completed
Last Updated

March 4, 2020

Status Verified

October 1, 2016

Enrollment Period

3 years

First QC Date

September 25, 2015

Last Update Submit

March 1, 2020

Conditions

Keywords

membrane sweepingdinoprostonemultiparaslabor inductioncesarean delivery

Outcome Measures

Primary Outcomes (1)

  • Vaginal delivery within 24 hours

    Vaginal delivery within 24 hours is defined as vaginal delivery after 24 hours of initiating intervention (i.e. membrane sweeping or dinoprostone) on the first day of induction.

    From the time of initiating intervention (i.e. membrane sweeping or dinoprostone) until the time of vaginal delivery, assessed up to 24 hours

Secondary Outcomes (3)

  • Successful labor induction

    From the time of initiating intervention (i.e. membrane sweeping or dinoprostone) until the time of active phase of labor (defined as a cervical dilatation of >=4cm), assessed up to 24 hours

  • Incidence of cesarean delivery

    End of labor induction (assessed up to 120 hours)

  • The interval from start of oxytocin to delivery

    From the time of initiating oxytocin infusion until the time of delivery, assessed up to 120 hours

Study Arms (2)

Oxytocin & Membrane sweeping

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

Drug: OxytocinProcedure: Membrane sweeping

Oxytocin & Dinoprostone

ACTIVE COMPARATOR

Women assigned to "Concurrent oxytocin with dinoprostone vaginal insert": The 10mg dinoprostone vaginal insert were placed in the posterior fornix for cervical ripening, followed by oxytocin infusion the next day

Drug: OxytocinDrug: Dinoprostone

Interventions

Oxytocin & DinoprostoneOxytocin & Membrane sweeping
Oxytocin & Dinoprostone
Oxytocin & Membrane sweeping

Eligibility Criteria

Sexfemale
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • singleton pregnancy
  • Multiparous women
  • gestational age \>=37.0 weeks
  • Bishop score \<=6
  • intact amniotic membrane
  • absence of labor
  • live fetus with vertex presentation
  • no previous uterine surgical procedure

You may not qualify if:

  • Multiple pregnancy
  • Placenta previa

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Obstetrics and Gynecology Seoul National University Bundang Hospital

Seongnam-si, Gyeonggi-do, 463-707, South Korea

Location

MeSH Terms

Interventions

OxytocinDinoprostone

Intervention Hierarchy (Ancestors)

Pituitary Hormones, PosteriorPituitary HormonesPeptide HormonesHormonesHormones, Hormone Substitutes, and Hormone AntagonistsPeptidesAmino Acids, Peptides, and ProteinsProstaglandins EProstaglandinsEicosanoidsFatty Acids, UnsaturatedFatty AcidsLipidsAutacoidsInflammation MediatorsBiological Factors

Study Officials

  • Kyo Hoon Park,, MD, PhD

    Seoul National University Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 25, 2015

First Posted

December 1, 2015

Study Start

October 1, 2015

Primary Completion

October 1, 2018

Study Completion

October 1, 2018

Last Updated

March 4, 2020

Record last verified: 2016-10

Locations