Uterocervical Angle in Induction of Labor
Uterocervical Angle in Success of Induction of Labor
1 other identifier
observational
150
1 country
1
Brief Summary
To evaluate the performance of uterocervical angle (UCA) in the prediction of labor induction.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Feb 2017
Shorter than P25 for all trials
1 active site
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
CompletedFirst Submitted
Initial submission to the registry
October 9, 2017
CompletedFirst Posted
Study publicly available on registry
October 12, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2018
CompletedMarch 6, 2018
March 1, 2018
1 year
October 9, 2017
March 3, 2018
Conditions
Keywords
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.
Interventions
uterocervical angle is the angle between lower segment of uterus and cervix
Eligibility Criteria
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)
Related Links
Study Officials
- STUDY DIRECTOR
Alev Aydin, MD,ObGyn
Kanuni SSTRH
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