Double Marker Test Price in Delhi
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Double Marker Test Price in Delhi – Lab Comparison
Compare Double Marker Test prices from leading diagnostic laboratories in Delhi. Review pricing, home sample collection availability, report turnaround time, and choose the laboratory that best meets your requirements.
📌 Prices are sourced from official laboratory and healthcare-platform websites and updated regularly.
💰 Starts at ₹1390 | 🧪 Multiple Labs Compared
🚗 Home Collection | 🏅 NABL Status Shown
📅 Last Updated: 20 August 2026
👆 Tap the Price header to see the lowest or highest price first.| Lab Name | Price(sort) | Book | Report Time | Home Collection | Parameters | NABL |
|---|---|---|---|---|---|---|
| Meditest | Cheapest ₹1390 | Book Test → | within 2 days | ✅ Yes | - | ✅ Yes |
| Neuberg Diagnostics | ₹1400 | Book Test → | 1 day | ✅ Yes (in most areas) | 3 | ✅ Yes |
| Ganesh Diagnostic | ₹1425 | Book Test → | within 24 hours | ✅ Yes | - | ✅ Yes |
| HOD | ₹1499 | Book Test → | next day | ✅ Yes | 2 | ✅ Yes |
| Core Lab | ₹1499 | Book Test → | within 2 days | ✅ Yes | - | ✅ Yes |
| PharmEasy (Platform) | ₹1699 | Book Test → | within 28 hours | ✅ Yes | 3 | N/A |
| Qris Health | ₹1859 | Book Test → | within 24 hours | ✅ Yes | - | ✅ Yes |
| Healthians | ₹1917 | Book Test → | within 48 hours | ✅ Yes | 1 | ✅ Yes |
| Redcliffe Lab | ₹1999 | Book Test → | within 42 hours | ✅ Yes | 2 | ✅ Yes |
| City X-Ray & Clinic | ₹2100 | Book Test → | within 24 hours | ✅ Yes | - | ✅ Yes |
| Manipal TRUtest | ₹2100 | Book Test → | within 48 hours | ✅ Yes | - | ✅ Yes |
| 1 Mg (Platform) | ₹2160 | Book Test → | within 33 hours | ✅ Yes | - | N/A |
| HR Diagnostic | ₹2300 | Book Test → | within 48 hours | ✅ Yes | - | ✅ Yes |
| Dr Lal Path Labs | ₹2360 | Book Test → | same day | ✅ Yes | - | ✅ Yes |
| Max Lab | ₹2400 | Book Test → | - | ✅ Yes | 4 | ✅ Yes |
| Orange Health Labs | ₹2400 | Book Test → | within 3 days | ✅ Yes | 2 | ✅ Yes |
| Niramaya PathLabs | ₹2420 | Book Test → | within 3 days | ✅ Yes | - | ✅ Yes |
| Mahajan Imaging and Labs | ₹2450 | Book Test → | same day | ✅ Yes | 1 | ✅ Yes |
| MetroPolis | ₹2500 | Book Test → | within 24 hours | ✅ Yes | - | ✅ Yes |
| Thyrocare | ₹2605 | Book Test → | within 55 hours | ✅ Yes | 3 | ✅ Yes |
| Agilus Diagnostic(SRL) | ₹2750 | Book Test → | next day | ✅ Yes | 8 | ✅ Yes |
| Max at Home | ₹2976 | Book Test → | next day | ✅ Yes | - | ✅ Yes |
| Apollo 24/7 (Platform) | ₹3449 | Book Test → | within 96 hours | ✅ Yes | - | N/A |
Note: This comparison includes the standard Double Marker Test (Free Beta hCG + PAPP-A) performed during the first trimester of pregnancy. It does not include NT Scan, NIPT, Triple Marker Test, Quadruple Marker Test, or other prenatal screening packages.
Compare Other Blood Tests
What is a Double Marker Test?
A Double Marker Test is a prenatal blood test performed during the first trimester of pregnancy to assess the risk of certain chromosomal conditions in the developing baby. The test measures two substances in the mother’s blood: Free Beta hCG (Human Chorionic Gonadotropin) and Pregnancy-Associated Plasma Protein A (PAPP-A).
The Double Marker Blood Test is usually performed between 11 and 13 weeks + 6 days of pregnancy and is commonly combined with an NT (Nuchal Translucency) ultrasound scan as part of first-trimester screening. However, this page compares the blood test only.
A Double Marker Test is a screening test, not a diagnostic test. It estimates the risk of certain chromosomal abnormalities, and the results are interpreted together with the mother’s age, ultrasound findings, and other clinical information. If the screening result indicates an increased risk, your healthcare provider may recommend additional diagnostic tests.
Why is a Double Marker Test Done?
A Double Marker Test is performed during the first trimester of pregnancy to estimate the risk of certain chromosomal abnormalities in the developing baby. It is a screening test that helps identify pregnancies that may require further evaluation.
A healthcare provider may recommend a Double Marker Blood Test to:
- Assess the risk of chromosomal conditions such as Down syndrome (Trisomy 21) and Edwards syndrome (Trisomy 18).
- Perform first-trimester prenatal screening between 11 and 13 weeks + 6 days of pregnancy.
- Support risk assessment when combined with the NT (Nuchal Translucency) ultrasound scan.
- Help determine whether additional tests, such as NIPT or diagnostic procedures, may be appropriate based on the screening result.
- Provide information that supports prenatal counseling and pregnancy management.
A Double Marker Test does not diagnose a chromosomal condition. The results indicate whether the pregnancy is at low risk or high risk, and your doctor interprets them together with your age, ultrasound findings, medical history, and other clinical information.
What Does a Double Marker Test Measure?
A Double Marker Test measures the levels of two pregnancy-related markers in the mother’s blood:
- Free Beta hCG (Human Chorionic Gonadotropin)
- Pregnancy-Associated Plasma Protein A (PAPP-A)
The laboratory analyzes these markers along with factors such as the mother’s age, gestational age, and, when available, NT (Nuchal Translucency) ultrasound findings to estimate the risk of certain chromosomal abnormalities in the developing baby.
A Double Marker Blood Test does not detect or diagnose a chromosomal condition. Instead, it calculates the probability that the pregnancy is at low risk or high risk for specific conditions. If the screening result indicates an increased risk, your healthcare provider may recommend additional screening or diagnostic tests.
Who Should Get a Double Marker Test?
A Double Marker Test is generally recommended for pregnant women during the first trimester as part of routine prenatal screening for certain chromosomal abnormalities.
A doctor may recommend a Double Marker Blood Test if you:
- Are between 11 and 13 weeks + 6 days of pregnancy.
- Want first-trimester screening for certain chromosomal conditions.
- Have an increased maternal age or other factors that may increase the risk of chromosomal abnormalities.
- Have a family or previous pregnancy history of certain chromosomal disorders.
- Have been advised to undergo combined first-trimester screening along with an NT (Nuchal Translucency) scan.
- Require further risk assessment before considering additional screening or diagnostic tests.
A Double Marker Test should always be interpreted together with your gestational age, maternal age, ultrasound findings, medical history, and other clinical information.
Double Marker Test Normal Range
Unlike many blood tests, a Double Marker Test does not have a single normal range. The results are interpreted using a risk calculation that considers the mother’s age, gestational age, blood marker levels, and, when available, NT (Nuchal Translucency) ultrasound findings.
| Screening Result | Interpretation |
|---|---|
| Low Risk | Lower probability of the screened chromosomal conditions. Routine prenatal care is usually continued. |
| High Risk | Higher probability of the screened chromosomal conditions. Your doctor may recommend additional screening or diagnostic tests. |
A Double Marker Test is a screening test, not a diagnostic test. A high-risk result does not confirm that the baby has a chromosomal condition, and a low-risk result does not completely rule it out. The results should always be interpreted by your healthcare provider in the context of your pregnancy.
Double Marker Test Preparation
A Double Marker Test usually requires little or no special preparation. However, following your healthcare provider’s instructions can help ensure accurate risk assessment.
- Fasting: Fasting is generally not required for a Double Marker Blood Test.
- Gestational Age: The test should be performed between 11 weeks and 13 weeks + 6 days of pregnancy for accurate screening.
- Medical Information: Inform your healthcare provider about your pregnancy history, current medications, and any existing medical conditions.
- Ultrasound Details: If an NT (Nuchal Translucency) scan has already been performed, ensure the results are available, as they may be used together with the blood test for combined first-trimester screening.
- Other Tests: Follow any additional instructions provided by your doctor or diagnostic laboratory.
Do not stop taking any prescribed medicines unless your healthcare provider specifically advises you to do so.
How is a Double Marker Test Performed?
A Double Marker Test is performed using a blood sample collected from a vein in the mother’s arm.
- A healthcare professional cleans the skin over a vein in your arm.
- A small needle is inserted into the vein to collect a blood sample.
- The blood sample is sent to a laboratory for analysis.
- The laboratory measures the levels of Free Beta hCG and Pregnancy-Associated Plasma Protein A (PAPP-A).
- The results are combined with your gestational age, maternal age, and, when available, NT (Nuchal Translucency) ultrasound findings to estimate the risk of certain chromosomal abnormalities.
The blood collection procedure usually takes only a few minutes, and most pregnant women can resume their normal daily activities immediately after the test.
What Do High-Risk and Low-Risk Double Marker Test Results Mean?
Low-Risk Result
A low-risk Double Marker Test result indicates a lower probability that the baby has the chromosomal conditions screened by the test, such as Down syndrome (Trisomy 21) or Edwards syndrome (Trisomy 18). In most cases, routine prenatal care continues as advised by your healthcare provider.
High-Risk Result
A high-risk Double Marker Test result indicates a higher probability of one or more of the chromosomal conditions included in the screening. It does not confirm that the baby has a chromosomal abnormality.
If your Double Marker Test result is reported as high risk, your doctor may recommend additional screening or diagnostic tests, such as NIPT, chorionic villus sampling (CVS), or amniocentesis, depending on your individual clinical situation.
A Double Marker Test is a screening test, and its results should always be interpreted together with your gestational age, maternal age, ultrasound findings, medical history, and other clinical information.
What Conditions Can a Double Marker Test Help Assess?
A Double Marker Test is a prenatal screening test that helps assess the risk of certain chromosomal abnormalities in the developing baby. Doctors interpret the results together with your gestational age, maternal age, NT (Nuchal Translucency) ultrasound findings, and other clinical information.
A Double Marker Blood Test may help assess the risk of:
- Down syndrome (Trisomy 21).
- Edwards syndrome (Trisomy 18).
- Certain other chromosomal abnormalities, when interpreted as part of combined first-trimester screening.
- Pregnancies that may benefit from additional screening or diagnostic testing.
A Double Marker Test does not diagnose any chromosomal condition. It estimates the probability of specific conditions and helps identify pregnancies that may require further evaluation using tests such as NIPT, CVS, or amniocentesis, when clinically appropriate.
Advantages of a Double Marker Test
A Double Marker Test is a non-invasive prenatal screening test that helps assess the risk of certain chromosomal abnormalities during the first trimester of pregnancy. It provides valuable information that can help healthcare providers decide whether additional screening or diagnostic tests may be needed.
Key advantages include:
- Helps assess the risk of Down syndrome (Trisomy 21) and Edwards syndrome (Trisomy 18).
- Can be performed during the first trimester (11–13 weeks + 6 days) of pregnancy.
- Uses a simple blood sample and is non-invasive.
- Supports risk assessment when combined with an NT (Nuchal Translucency) ultrasound.
- Helps identify pregnancies that may benefit from additional screening or diagnostic testing.
- Assists healthcare providers in planning appropriate prenatal care based on the screening results.
A Double Marker Test is a screening test, not a diagnostic test. The results should always be interpreted together with your gestational age, maternal age, ultrasound findings, medical history, and other clinical information.
Frequently Asked Questions
What is the Double Marker Test Price in Delhi?
The Double Marker Test price in Delhi typically ranges from ₹1200 to ₹4000, depending on the diagnostic laboratory, report turnaround time, and ongoing offers. CostKlaro helps you compare Double Marker Test prices across trusted laboratories in Delhi.
What is a Double Marker Test?
A Double Marker Test is a first-trimester prenatal blood test that measures Free Beta hCG and PAPP-A (Pregnancy-Associated Plasma Protein A) to estimate the risk of certain chromosomal abnormalities in the developing baby.
When is a Double Marker Test done?
A Double Marker Test is usually performed between 11 weeks and 13 weeks + 6 days of pregnancy as part of first-trimester prenatal screening.
Is fasting required for a Double Marker Test?
No. Fasting is generally not required for a Double Marker Blood Test unless your healthcare provider or laboratory advises otherwise.
What sample is required for a Double Marker Test?
A blood sample collected from a vein in the mother’s arm is required for a Double Marker Test.
How long does it take to get the Double Marker Test report?
Most diagnostic laboratories provide the Double Marker Test report within 1 to 3 days, although the exact turnaround time may vary between laboratories.
What does a low-risk Double Marker Test result mean?
A low-risk result indicates a lower probability of the chromosomal conditions screened by the test. It does not completely rule out these conditions, and the result should always be interpreted by your healthcare provider.
What does a high-risk Double Marker Test result mean?
A high-risk result indicates a higher probability of certain chromosomal abnormalities. It does not confirm a diagnosis, and your doctor may recommend additional screening or diagnostic tests.
Can a Double Marker Test diagnose Down syndrome?
No. A Double Marker Test is a screening test, not a diagnostic test. It estimates the risk of Down syndrome (Trisomy 21) and certain other chromosomal conditions but cannot confirm them.
What conditions does a Double Marker Test screen for?
A Double Marker Test primarily screens for Down syndrome (Trisomy 21) and Edwards syndrome (Trisomy 18) as part of first-trimester prenatal screening.
Is a Double Marker Test safe during pregnancy?
Yes. A Double Marker Test is a routine blood test and is considered safe during pregnancy. It requires only a blood sample from the mother and does not directly affect the baby.
Is an NT scan required with a Double Marker Test?
A Double Marker Test is often interpreted together with an NT (Nuchal Translucency) ultrasound scan as part of combined first-trimester screening. Your healthcare provider will advise whether both tests are recommended in your situation.
Who should get a Double Marker Test?
A Double Marker Test is generally recommended for pregnant women between 11 and 13 weeks + 6 days of pregnancy as part of first-trimester prenatal screening.
What is the difference between a Double Marker Test and NIPT?
A Double Marker Test is a screening test that estimates the risk of certain chromosomal abnormalities using blood markers, while NIPT (Non-Invasive Prenatal Testing) analyzes fetal DNA in the mother’s blood and generally offers higher screening accuracy. Your healthcare provider can help determine which test is appropriate.
How can I compare Double Marker Test prices in Delhi?
CostKlaro allows you to compare Double Marker Test prices, home sample collection availability, report turnaround time, and trusted diagnostic laboratories in Delhi, helping you choose the right test at the best available price.
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Sources & References
The information on this page has been compiled from official diagnostic laboratory websites, publicly available healthcare resources, and reputable medical references. Test prices, home sample collection availability, and report delivery times may change over time. We recommend verifying the latest information directly with the diagnostic laboratory before booking your test. Costklaro aims to provide transparent, accurate, and regularly updated healthcare information to help users make informed decisions.
- Official websites of the diagnostic laboratories listed in the comparison table
- National Health Authority (NHA), Government of India
- Indian Council of Medical Research (ICMR), where applicable
- National Institutes of Health (NIH) and other internationally recognized medical references, where applicable