Pre-Eclampsia Prediction By Doppler Screening Of Uterine Arteries And Angiogenic Factors In Second Trimester Of Pregnancy
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|ClinicalTrials.gov Identifier: NCT00725660|
Recruitment Status : Unknown
Verified July 2008 by Shaare Zedek Medical Center.
Recruitment status was: Not yet recruiting
First Posted : July 30, 2008
Last Update Posted : July 30, 2008
BACKGROUND: Pre-eclampsia complicates about 2% of pregnancies. It accounts for at least 50 000 maternal deaths per year worldwide and is the second most common cause of maternal death in the developing world. Also, Pre-eclampsia is the commonest cause of iatrogenic prematurity, It frequently coexists with intrauterine growth restriction (IUGR) and placental abruption, other important causes of adverse prenatal outcome.
There have been many studies investigating whether the disease can be prevented. In order to achieve this, one needs to be able to identify firstly those women that are at highest risk of the disease.
Early studies showed that impedance to flow in the uterine arteries decreases with gestation in normal pregnancies, while in pregnancies with established pre-eclampsia or IUGR the impedance is increased.
These observations led to a number of screening studies in the second trimester, which assessed if it is possible to predict those pregnancies destined to have complications of impaired placentation. These studies showed that women with increased impedance to uterine artery blood flow have an increased risk of developing pre-eclampsia, and detection can be further increased by using angiogenic factors (That are involved in the pathogenesis of Pre- eclampsia and could be useful for early prediction of the disease: VEGF, PIGF, PP13, sFLT1) in combination with uterine arteries Doppler study in the second trimester.
METHODS: In this study we would like to add uterine arteries Doppler to the early routine detailed ultrasound examination (14-16 weeks), in 3000 women in Jerusalem. in addition we would like to check angiogenic factors from the serum blood taken for the routine triple test in these women (16-18 weeks).pregnancy outcome would be collected after labour from the medical centers participating in this research.
|Condition or disease|
|Pregnancy Pre Eclampsia|
|Study Type :||Observational|
|Estimated Enrollment :||3000 participants|
|Study Start Date :||September 2008|
Pregnant women in second trimester that took the routine triple test, and are having an early routine detailed ultrasound examination.
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): NCT00725660
|Contact: Eyal Mazaki, MDfirstname.lastname@example.org|
|Shaare Zedek Medical Center||Not yet recruiting|
|Contact: Eyal Mazaki, MD 972-2-6555555 email@example.com|
|Principal Investigator: Eyal Mazaki, MD|