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Establishing First Trimester Markers for the Identification of High Risk Twin

Establishing First Trimester Sonographic, Biochemical and Clinical Markers for the Identification of High Risk Twin in the First Trimester

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02031393
Enrollment
300
Registered
2014-01-09
Start date
2009-09-30
Completion date
2014-07-31
Last updated
2014-01-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pre-Eclampsia, Small for Gestational Age (Disorder)

Brief summary

The purpose of this study is to determine whether we can establish different markers suc as mean arterial pressure , flow in the uterine arteries, biochemical markers in maternal blood and more un the first trimester, in order to screen for twin pregnancies that are more likely to develop adverse pregnancy outcome: early delivery, pre eclampsia or small fetuses.

Interventions

None listed

Sponsors

Assaf-Harofeh Medical Center
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* pregnant women from 11 -14 weeks of gestation

Exclusion criteria

* nuchal thickness above 3 mm, * Chronic hypertension, * thrombophilia, * Diabetes

Design outcomes

Primary

MeasureTime frameDescription
The development of preeclampsiaafter deliverythe women will be approached after birth to asses whether they developed preeclampsia or pregnancy induced hypertension

Secondary

MeasureTime frame
intra uterine growth restrictionafter delivery

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026