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Aari Fetal Centre

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First trimester Combined Test

The First Trimester Combined Test is a prenatal screening assessment performed during early pregnancy, usually between 11 weeks and 13 weeks + 6 days. It combines an ultrasound examination, including nuchal translucency (NT) measurement, with maternal blood tests and relevant pregnancy information to estimate the chance of certain chromosomal conditions.

Early Prenatal Screening

NT Ultrasound Assessment

Combined Risk Assessment

First trimester Combined Test

Nuchal Translucency Measurement
Fetal Growth & Measurements
Fetal Cardiac Activity
Early Fetal Anatomy
Maternal Blood Tests
Maternal Information
Chromosomal Risk Screening
Multiple Pregnancy Assessment
Pregnancy Dating

Important Information

The First Trimester Combined Test is a screening test, not a diagnostic test. A higher-chance result does not confirm that the baby has a chromosomal condition, while a lower-chance result cannot completely exclude one.
  • The test estimates risk for selected chromosomal conditions and does not provide a definitive diagnosis.
  • A higher-chance result may require further screening or diagnostic testing.
  • Diagnostic testing may include procedures such as chorionic villus sampling or amniocentesis.
  • A lower-chance result does not guarantee that the baby has no genetic, chromosomal or structural condition.
  • The quality of the ultrasound assessment can be affected by fetal position, gestational age and other factors.
  • The combined test does not replace the detailed mid-trimester anomaly scan.
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