Uterocervical Angle Versus Cervical Length as a Predictor of Labor Induction in Term Singleton Pregnancy
Uterocervical and Posterior Cervical Angle Versus Cervical Length and Bishop's Score as a Predictor of Labor Induction in Term Singleton Pregnancy: a Prospective Study
1 other identifier
observational
140
1 country
1
Brief Summary
Induction of labor is frequently performed in all obstetric clinics. Failed IOL has been defined in many different ways.Bishop scoring, which is a traditional and subjective method, is more frequently evaluated with cervical length, which has taken its place in preterm labor, and various ultrasonographic evaluations such as Uterocervical angle (UCA), Posterior cervical angle (PCA), cervical elastography, transvulvar ultrasonography, which have recently increased in popularity, have gained importance and led us to evaluate these parameters in our clinic. The relationship between the angles between the uterus and cervix and labor has been known for some time.
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 Jun 2024
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
June 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
August 2, 2024
CompletedFirst Submitted
Initial submission to the registry
August 14, 2024
CompletedFirst Posted
Study publicly available on registry
August 16, 2024
CompletedAugust 20, 2024
August 1, 2024
2 months
August 14, 2024
August 16, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
The efficacy of uterocervical angle
The efficacy of uterocervical angle in predicting labor induction success in nulliparous patients at term.
2 days
Study Arms (2)
group 1
delivered vaginally with successful induction of labor
group 2
failed induction and delivered with C/S
Interventions
With the patient in the lithotomy position and empty bladder, care was taken to avoid applying pressure to the cervix with the transvaginal probe. The cervix was aligned in the midline, and the endocervical canal was visualized throughout its length.During cervical measurement, care was taken to ensure that the internal os, external os, and entire endocervical canal were visible in the same image. With the endocervical canal, external os, and internal os linearly displayed on the screen, the angle between the endocervical canal, anterior and posterior uterine segment was measured using the ultrasound's "angle measurement" feature.For the measurement of the uterocervical angle, the first line of the angle was defined along the endocervical canal used for measuring cervical length, and the second line was drawn from the internal os along the anterior uterine segment for a minimum of two centimeters. The angle between these two lines was recorded as the uterocervical angle in the form.
Eligibility Criteria
This prospective observational study was conducted at the Department of Obstetrics and Gynecology, Ankara Etlik Hospital, between June 2024 and August 2024, on 140 term pregnancies admitted for maternal or fetal reasons , planned for labor induction.
You may qualify if:
- weeks and older Nulliparity Live, singular Verteks presentation Cervical opening\<3 cm Bishop score\<7 Patients not in active action
You may not qualify if:
- Presence of contraindications to vaginal delivery (pls previa, detached pls...)
- History of previous uterine surgery
- Multiple pregnancies
- Non-vertex presentation
- Uncontrolled HT Uncontrolled DM
- Fetal distress
- Macrosomic fetus Patients in active labor
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Etlik Zubeyde Hanım Women's Health Education Hospital
Ankara, 06000, Turkey (Türkiye)
Study Officials
- STUDY CHAIR
Ali Turhan ÇAĞLAR
Etlik Zübeyde Hanım EAH
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Target Duration
- 2 Days
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Medical doctor, Specialist of gynecology and obstetrics
Study Record Dates
First Submitted
August 14, 2024
First Posted
August 16, 2024
Study Start
June 1, 2024
Primary Completion
August 1, 2024
Study Completion
August 2, 2024
Last Updated
August 20, 2024
Record last verified: 2024-08