The Association Between Uterine Artery Notch and First Trimester Bleeding
NCT ID: NCT01069406
Last Updated: 2015-05-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
200 participants
OBSERVATIONAL
2010-03-31
2012-05-31
Brief Summary
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A prospective study is designed and two groups will be studied; patients with abnormal uterine artery Doppler at second trimester (study group) and patient with normal uterine artery Doppler at second trimester (control group).The patients will be asked, as part of the routine history taken before the US about having first trimester bleeding during the current pregnancy.
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Detailed Description
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A prospective study is designed and two groups will be studied; patients with abnormal uterine artery Doppler at second trimester (study group) and patient with normal uterine artery Doppler at second trimester (control group). Both the study group and the control group represent high risk pregnant patients and the Doppler flows are done as part of the patient's predictive risk for placental associated abnormalities. The patients will be asked, as part of the routine history taken before the US about having first trimester bleeding during the current pregnancy.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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presence of uterine artery notch
patients with uterine artery notch during the 2nd and 3rd trimester
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Patients without known gestational age (according to last month period or first trimester ultrasound
* Pregnancies with congenital structural or chromosomal anomalies
* Lack of prenatal care
FEMALE
Yes
Sponsors
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Soroka University Medical Center
OTHER
Responsible Party
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Gali Pariente
Dr
Locations
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Us unit
Soroka Medical Center, Beer Sheva, Israel
Countries
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Other Identifiers
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sor493710CTIL
Identifier Type: -
Identifier Source: org_study_id
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