Here you can find answers to the most common questions in relation to EVITA TEST COMPLETE. If you do not find the answer to your specific question, do not hesitate to reach out to us. Find our contact information below.
The five most common questions:
You can take the test when you are in the pregnancy weeks of 10+0 to 14 + 6.
Please contact one of our partner clinics and book a time to have a blood sample taken.
You will have the result of the test for chromosomal aberrations within 12 working days.
The difference between the conventional NIPT test, also referred to as cell-free NIPT (cfNIPT), and EVITA TEST COMPLETE is that cfNIPT analyses fragments of fetal DNA circulating in maternal blood. These fetal DNA fragments are contaminated with maternal DNA, hence limiting the resolution of analysis. EVITA TEST COMPLETE uses a technology to isolate fetal cells from maternal blood and analyse pure fetal DNA. Hence, EVITA TEST COMPLETE has the ability to detect smaller changes in the fetal DNA.
EVITA TEST COMPLETE is a screening test that examines for chromosomal abnormalities in the form of aneuploidies in the fetus such as Trisomy 21 (Down syndrome), and for copy number variations (microdeletions and microduplications). If chromosomal abnormalities are detected by an EVITA TEST COMPLETE, an invasive diagnostic test such as Chorionic Villus Sampling (CVS) is always recommended to verify the finding.
A CVS is a diagnostic analysis and is typically offered in pregnancy weeks 10-12, if there is a risk that the fetus has chromosomal aneuploidies. The CVS has an even better resolution, as it is based on the analysis of tissue biopsy, and thus it is possible to find even smaller copy number variations in the fetus.
Yes, you can get information about the sex of your child. The information can be provided to you when you are in 12th pregnancy week or more. Please inform the staff at our partner clinic about your request.
The first trimester screening based on my age, the maternal serum blood test (double test) as well as fetal nuchal translucency have shown that I am in the low risk. Can I still benefit from the EVITA TEST COMPLETE?
Yes, the first trimester screening is performed to assess the risk of the most common trisomies, especially Trisomy 21 (Down syndrome). Small changes of the DNA may not be detected in these screenings.
EVITA TEST COMPLETE, which analyses pure fetal DNA, has the necessary technology to detect small changes in the DNA. All relevant findings in the analyses of the fetal DNA will be informed to you.
The result of the test will be sent to the clinic where you have had your sample taken.
If a chromosomal aberration is detected, we advise you to contact your GP to arrange the further course.
All results are being analysed by clinical geneticists with many years’ experience within genetic results from fetal cells. All relevant findings of the analysis of the fetal DNA will be communicated to you.
Yes, you can. Please contact one of our partner clinics or contact us at email@example.com, and we will provide you with information about the nearest clinic.
The price of the EVITA TEST COMPLETE is DKK 12,000.
If you would like to know even more about the EVITA TEST COMPLETE, please call us on +45 93 96 00 00. We are open Monday-Friday from 8 AM – 4 PM CET and our team will be happy to answer any questions you may have. You are also welcome to write your question in the form and we will answer within 24 hours.