NCT03308656

Brief Summary

To evaluate the performance of uterocervical angle (UCA) in the prediction of labor induction.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
150

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Feb 2017

Shorter than P25 for all trials

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

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2017

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

October 9, 2017

Completed
3 days until next milestone

First Posted

Study publicly available on registry

October 12, 2017

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2018

Completed
Last Updated

March 6, 2018

Status Verified

March 1, 2018

Enrollment Period

1 year

First QC Date

October 9, 2017

Last Update Submit

March 3, 2018

Conditions

Keywords

uterocervical angle, labor induction

Outcome Measures

Primary Outcomes (1)

  • uterocervical angle

    the angle between the lower segment of uterus and cervix

    once at the beginning of enrollment

Study Arms (1)

Induced labor in term pregnancies

100 singleton nulliparous patients are planning to complete the study period. Study group constitute of third trimester pregnancies between 37-40 weeks of gestation. All participants were nulliparous and had no systemic illnesses. The uterocervical angle will be measured in all participants before the induction of labor.

Other: uterocervical angle

Interventions

uterocervical angle is the angle between lower segment of uterus and cervix

Induced labor in term pregnancies

Eligibility Criteria

Age18 Years - 40 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Pregnant population undergoing labor induction in the third trimester

You may qualify if:

  • Nulliparous singleton pregnancy
  • no previous systemic illnesses

You may not qualify if:

  • abnormal Pap smear
  • previous cesarean section
  • history of dilatation and curettage (D\&C)
  • history of LEEP and cervical conization

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kanuni SSTRH

Istanbul, 34303, Turkey (Türkiye)

Location

Related Links

Study Officials

  • Alev Aydin, MD,ObGyn

    Kanuni SSTRH

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
MD, Director of labor room

Study Record Dates

First Submitted

October 9, 2017

First Posted

October 12, 2017

Study Start

February 1, 2017

Primary Completion

February 1, 2018

Study Completion

February 1, 2018

Last Updated

March 6, 2018

Record last verified: 2018-03

Data Sharing

IPD Sharing
Will not share

Locations