Pre-Eclampsia Prediction By Doppler Screening Of Uterine Arteries And Angiogenic Factors In Second Trimester Of Pregnancy
Recruitment status was Not yet recruiting
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Purpose
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 |
|---|
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Pregnancy Pre Eclampsia |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Estimated Enrollment: | 3000 |
| Study Start Date: | September 2008 |
| Groups/Cohorts |
|---|
|
1
Pregnant women in second trimester that took the routine triple test, and are having an early routine detailed ultrasound examination.
|
Eligibility| Ages Eligible for Study: | 18 Years to 50 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Probability Sample |
Pregnant women in second trimester that took the routine triple test, and are having an early routine detailed ultrasound examination, in Jerusalem, Israel.
Inclusion Criteria:
- pregnant women in second trimester that took the routine triple test, and are having an early routine detailed ultrasound examination, in Jerusalem, Israel
Exclusion Criteria:
- none
Contacts and Locations| Contact: Eyal Mazaki, MD | 972-2-6555555 | eyalmazaki@hotmail.com |
| Israel | |
| Shaare Zedek Medical Center | Not yet recruiting |
| Jerusalem, Israel | |
| Contact: Eyal Mazaki, MD 972-2-6555555 eyalmazaki@hotmail.com | |
| Principal Investigator: Eyal Mazaki, MD | |
More Information
No publications provided
| Responsible Party: | DR. Eyal Mazaki, Shaare Zedek Medical Center Jerusalem Israel |
| ClinicalTrials.gov Identifier: | NCT00725660 History of Changes |
| Other Study ID Numbers: | 0153-08-HMO.CTIL |
| Study First Received: | July 29, 2008 |
| Last Updated: | July 29, 2008 |
| Health Authority: | Israel: The Israel National Institute for Health Policy Research and Health Services Research |
Keywords provided by Shaare Zedek Medical Center:
|
pre eclampsia doppler uterine |
arteries angiogenic factors |
Additional relevant MeSH terms:
|
Eclampsia Pre-Eclampsia Hypertension, Pregnancy-Induced Pregnancy Complications |
ClinicalTrials.gov processed this record on May 19, 2013