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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03828695
Other study ID # 10988
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2019
Est. completion date June 30, 2019

Study information

Verified date July 2019
Source Sanliurfa Mehmet Akif Inan Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To evaluate the performance of uterocervical angle (UCA) in the prediction of preterm labor in isolated polyhydramnios


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date June 30, 2019
Est. primary completion date June 30, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- isolated polyhydramnios pregnancies

- no previous systemic illnesses

Exclusion Criteria:

- abnormal Pap smear

- previous cesarean section

- history of dilatation and curettage (D&C)

- history of loop electrosurgical excision procedure (LEEP) and cervical conization

Study Design


Intervention

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

Locations

Country Name City State
Turkey Nefise N YENIGUL Sanliurfa

Sponsors (1)

Lead Sponsor Collaborator
Nefise Nazli YENIGUL

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary prediction of preterm birth by uterocervical angle in patients with idiopathic polyhydramnios. During the study period, women were enrolled and uterocervical angle were measured in the first evaluations of polyhydramnios patients in policlinics. Routine pregnancy follow-up was done by our team and weeks of delivery and maternal-fetal outcomes were noted. 6 month
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