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Evita Test Complete - NIPT test packaging

Evita Test Complete

 

Get the full overview of your child's chromosomes with Evita Test Complete – a fast, safe and accurate blood test for pregnant women.

Price 14500 DKK

 

Why choose Evita Test Complete?

 

  • The most detailed fetal genetic test on the market

  • Examines all of the fetus's chromosomes

  • Quick & risk-free – just a blood sample from the mother

  • Can be done from week 10+0 to 14+6

  • Includes gender determination at no extra cost

 

What are we testing for?

 

Evita Test Complete isolates whole fetal cells in the blood of the pregnant woman and can thus detect any chromosomal abnormalities in the fetus. The test screens for:


✔ Known chromosomal disorders such as Down syndrome & Edwards syndrome
✔ Rarer genetic syndromes that can have serious consequences for the child's development

With Evita Test Complete, you get the most accurate answer on the market to whether there is cause for concern about your child's genetic health.

🔗 Do you have any questions? Contact us or visit the Evita Test Complete website for more information.

Procedure:

  • Book an appointment for EVITA TEST COMPLETE from pregnancy week 10+0 to 14+6. However, we recommend booking as early as possible in case a repeat blood sample is needed (this must be taken no later than week 14+6).
    Please note: EVITA cannot be booked after Thursday at 12:00 noon, or on Fridays, Saturdays, and Sundays due to the laboratory schedule.

  • When you attend your appointment, the sonographer will provide information about the test, create your medical record, and perform an ultrasound scan to ensure that the pregnancy is progressing normally.

  • A blood sample is taken from the pregnant woman’s arm. The sample is sent for analysis and evaluation by a specialist physician in Denmark.

  • The results are sent to the clinic after approximately 12 working days, and you will be contacted by phone by our sonographer. The test results are subsequently shared with you by email.

  • If any abnormalities are detected in the test, you will be informed by our midwife, and we will arrange a referral for further prenatal diagnostics at the hospital.

In case of an inconclusive result

In a small number of samples (6%), there are not enough fetal cells in the blood sample to perform the chromosomal analysis.

In these cases, you will be offered a repeat blood sample free of charge (only within pregnancy weeks 10+0 to 14+6). After this, the proportion of samples in which chromosomal analysis cannot be completed is reduced to only 2%.

If you receive only some, but not all, test results, you will be charged for the full test. If you do not receive any test results at all, you will only be charged for the consultation and ultrasound scan. This means that we will refund the test fee to your account, minus DKK 1,000.

EVITA TEST COMPLETE is not validated for:

  • Twin pregnancies

  • Monogenic diseases (mutation in a single gene, e.g. cystic fibrosis)

  • Mosaicism (a small fraction of cells in the placenta or fetus has a chromosomal abnormality)

EVITA TEST COMPLETE cannot be used to test for:

  • Polyploidy (more than two copies of all chromosomes)

  • Balanced translocations (exchange of chromosomal material between two different chromosomes, with no change in the total amount of genetic material)

  • Uniparental disomy (UPD) (two copies of a chromosome inherited from only one parent)

 

Details about EVITA TEST COMPLETE comparison with other NIPT tests
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