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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03400358
Other study ID # 2016/12.5
Secondary ID
Status Completed
Phase N/A
First received January 6, 2018
Last updated March 3, 2018
Start date October 1, 2017
Est. completion date February 1, 2018

Study information

Verified date March 2018
Source Kanuni Sultan Suleyman Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To evaluate the uterocervical angle (UCA) in the prediction of second trimester termination success of multiparous women.


Description:

Medical termination of pregnancy 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 termination of second trimester pregnancy.The investigators focused on multiparous women who are taking Foley baloon for the cervical preparation and aim to measure their UCA.


Recruitment information / eligibility

Status Completed
Enrollment 148
Est. completion date February 1, 2018
Est. primary completion date January 31, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria:

- multiparous singleton pregnancy

- no previous systemic illnesses

Exclusion Criteria:

- abnormal Pap smear

- history of dilatation and curettage (D&C)

- history of LEEP and cervical conization

Study Design


Related Conditions & MeSH terms


Intervention

Other:
uterocervical angle
the angle between cervical canal and anterior uterine wall is measured sonographically.

Locations

Country Name City State
Turkey Kanuni SSTRH Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Kanuni Sultan Suleyman Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary uterocervical angle the angle between the cervical canal and anterior uterine wall 1 week
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