Placental Protein 13 Serum Endoglin and Uterine Doppler Indeces as Predictors of Pre-eclampsia
Maternal Serum Placental Protein 13 Serum Endoglin and Uterine Doppler Indeces as Predictors of Pre-eclampsia and Relation to Maternal and Neonatal Outcome
1 other identifier
observational
50
1 country
1
Brief Summary
50 pregnant females were divided in two groups, twenty five as a control group and twenty five as high risk group; they were subjected to uterine artery Doppler, measurement of maternal serum and detection of (MTHFR) gene polymorphisms in first trimester at 11 to 14 weeks of gestation, all pregnancies were followed until 40 weeks for development of pre-eclampsia
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jan 2015
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2015
CompletedFirst Submitted
Initial submission to the registry
January 26, 2015
CompletedFirst Posted
Study publicly available on registry
January 29, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2016
CompletedMarch 21, 2017
March 1, 2017
1.9 years
January 26, 2015
March 18, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
development of preeclampsia
40 weeks pregnancy
Study Arms (2)
preeclmapsia
women developed preeclampsia. ultrasound monitoring and uterine artery Doppler
control
women with normal blood pressure all through pregnancy. ultrasound monitoring and uterine artery Doppler
Interventions
Eligibility Criteria
pregnant women at 11 to 14 weeks of gestation
You may qualify if:
- pregnant women at 11 to 14 weeks of gestation
You may not qualify if:
- fetal anomalies other medical diseases as diabetes mellitus, renal or liver diseases
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
Kasr Alainy medical school
Cairo, Cairo Governorate, 12151, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ahmed Maged
Kasr Alainy medical school
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Target Duration
- 9 Months
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant professor
Study Record Dates
First Submitted
January 26, 2015
First Posted
January 29, 2015
Study Start
January 1, 2015
Primary Completion
December 1, 2016
Study Completion
December 1, 2016
Last Updated
March 21, 2017
Record last verified: 2017-03