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Uterocervical Angle in Induction of Labor

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ClinicalTrials.gov Identifier: NCT03308656
Recruitment Status : Completed
First Posted : October 12, 2017
Last Update Posted : March 6, 2018
Sponsor:
Information provided by (Responsible Party):
Berna Aslan Cetin, Kanuni Sultan Suleyman Training and Research Hospital

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

Condition or disease Intervention/treatment
Labor Induction, Third Trimester Other: uterocervical angle

Detailed Description:

Induction of labor is a common procedure in obstetrics. In recent years, uterocervical angle (UCA) emerged as a new ultrasound parameter in the prediction of labor. Dziadosz et al concluded that the performance of UCA was even better than the cervical length in their cohort. A wide UCA during second trimester shown to have an increased risk of preterm labor and narrow angle was less likely to have labor.

The investigators are aimed to investigate predictive role of both cervical length and UCA in the labor induction in third trimester of pregnancy.The investigators focused on nulliparous women who are taking dinoproston for the cervical preparation and aim to measure their UCA.

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Study Type : Observational
Actual Enrollment : 150 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Uterocervical Angle in Success of Induction of Labor
Actual Study Start Date : February 1, 2017
Actual Primary Completion Date : February 1, 2018
Actual Study Completion Date : February 1, 2018

Group/Cohort Intervention/treatment
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
uterocervical angle is the angle between lower segment of uterus and cervix




Primary Outcome Measures :
  1. uterocervical angle [ Time Frame: once at the beginning of enrollment ]
    the angle between the lower segment of uterus and cervix



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 40 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Pregnant population undergoing labor induction in the third trimester
Criteria

Inclusion Criteria:

  • Nulliparous singleton pregnancy
  • no previous systemic illnesses

Exclusion Criteria:

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03308656


Locations
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Turkey
Kanuni SSTRH
İstanbul, Turkey, 34303
Sponsors and Collaborators
Kanuni Sultan Suleyman Training and Research Hospital
Investigators
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Study Director: Alev Aydin, MD,ObGyn Kanuni SSTRH
Additional Information:
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Responsible Party: Berna Aslan Cetin, MD, Director of labor room, Kanuni Sultan Suleyman Training and Research Hospital
ClinicalTrials.gov Identifier: NCT03308656    
Other Study ID Numbers: 2017/239
First Posted: October 12, 2017    Key Record Dates
Last Update Posted: March 6, 2018
Last Verified: March 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Berna Aslan Cetin, Kanuni Sultan Suleyman Training and Research Hospital:
uterocervical angle, labor induction