Double Marker Test Cost in India

The double marker test measures two substances in the mother’s blood: free beta-hCG and PAPP-A. These markers, when analysed along with details such as the mother’s age and the NT scan findings, help estimate the chances of certain chromosomal conditions in the baby. The test mainly screens for:

• Down syndrome (Trisomy 21)
• Edwards syndrome (Trisomy 18)
• Patau syndrome (Trisomy 13)
  

This test is not meant to diagnose a condition. It only gives an overall risk estimate so that the doctor can decide if further tests are needed.

Why is the Double Marker Test Important?

This test gives parents early clarity during pregnancy. It helps identify possible concerns at a stage when more detailed tests can still be done comfortably. Early screening also brings peace of mind, which is valuable in the first trimester.

Several elements influence the cost of the double marker test in pregnancy across India:

• The city or region where the test is done
• Whether it is done at a private hospital, maternity centre, or diagnostic lab
• If the test is done along with the NT scan
• The quality of equipment and the level of accreditation of the laboratory
• Home sample collection charges, if availed
  

When booked together, the cost of the NT scan and double marker test is often between ₹3,000 and ₹6,000.

When is the Double Marker Test Done?

Doctors usually recommend the double marker test between weeks 9 and 13 of pregnancy. The ideal time is commonly between week 11 and week 13, when the NT scan is also scheduled.

Who Should Get the Double Marker Test?

Although the double marker test is offered to most pregnant women, it is especially recommended for:

• Women who are above 30 years of age
• Pregnancies conceived through IVF
• Women with a history of chromosomal conditions in the family
• Those who had previous pregnancy complications
• Anyone whose doctor wants a more detailed early screening
  

There is no special preparation required. You can eat and drink normally. The only important thing is to share your correct pregnancy week and medical history with the doctor or lab, because these details are used while interpreting the double marker test results.

How is the Double Marker Test Done?

The double marker test is a simple blood test. A technician collects a blood sample from your arm. The sample is analysed in the lab, and the results are usually ready within two to four days. Many hospitals also share double marker test normal report images for easier understanding.

Understanding the Double Marker Test Results

Your double marker test report compares the hormone levels with the expected range for your stage of pregnancy. The final report classifies the risk as:

• Low risk: Suggests that the chances of a chromosomal condition are minimal
• High risk: Suggests that further tests like NIPT or CVS may be advised

The report must always be interpreted by a gynaecologist, because the numbers depend on age, gestational week, and NT scan findings.

People trust Birla Fertility and IVF for:

• Reliable and accurate double marker blood testing
• Experienced fetal medicine specialists
• High-quality ultrasound imaging for NT scans
• Transparent pricing with no hidden charges
• Guidance on your double marker test results and next steps

The focus is always on supportive care, timely screening, and clear communication.