- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03828695
Uterocervical Angle in Idiopathic Polyhydramnios
July 21, 2019 updated by: Nefise Nazlı YENIGUL
Efficacy and Efficiency of Uterocervical Angle for Prediction of Preterm Labor in Patients With Idiopathic Polyhydramnios: a Prospective Cohort Study
To evaluate the performance of uterocervical angle (UCA) in the prediction of preterm labor in isolated polyhydramnios
Study Overview
Study Type
Interventional
Enrollment (Actual)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Sanlıurfa, Turkey
- Nefise N YENIGUL
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 45 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: SCREENING
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
OTHER: uterocervical angle
uterocervical angle is the angle between lower segment of uterus and cervix
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uterocervical angle is the angle between lower segment of uterus and cervix
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
prediction of preterm birth by uterocervical angle in patients with idiopathic polyhydramnios.
Time Frame: 6 month
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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.
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6 month
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
January 1, 2019
Primary Completion (ACTUAL)
June 30, 2019
Study Completion (ACTUAL)
June 30, 2019
Study Registration Dates
First Submitted
January 30, 2019
First Submitted That Met QC Criteria
January 31, 2019
First Posted (ACTUAL)
February 4, 2019
Study Record Updates
Last Update Posted (ACTUAL)
July 23, 2019
Last Update Submitted That Met QC Criteria
July 21, 2019
Last Verified
July 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 10988 (DAIDS ES Registry Number)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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