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SickleClear™ NIPT: Clarity. Confidence. Built for Africa
For parents in Nigeria and across the continent, the risk of Sickle Cell Disease (SCD) is a profound reality. With nearly 1 in 4 Nigerians carrying the sickle trait, the need for safe, accurate, and early prenatal screening is not just clinical—it’s personal.
You deserve to know your baby’s risk early, without compromising the pregnancy you cherish.
Introducing SickleClear™ NIPT—the Non-Invasive Prenatal Test specifically engineered for high-prevalence settings and validated on African genotypes.
The Safe Answer to a Critical Question
What is SickleClear™ NIPT?
SickleClear™ is a sophisticated blood test that screens your unborn baby for the Sickle Cell mutation (HbS) as early as 10 weeks of gestation.
It works by analyzing minute fragments of your baby’s DNA (cfDNA) circulating safely in your maternal blood. This innovative approach replaces the need for risky, invasive procedures.
Why SickleClear™ is the Essential Choice:
Designed for Parents-at-Risk
Who Should Choose SickleClear™?
- Couples where one or both partners are known AS (carrier) or SS (affected).
- Pregnant women who require early, definitive insight into their baby’s HbS risk to plan the remainder of their antenatal journey.
What Your Report Will Tell You:
SickleClear™ delivers a clear risk assessment, not merely a statistical probability.
- High-Risk for Fetal HbSS (Affected)
- Low-Risk for Fetal HbSS (Unaffected or Carrier)
- Note: Results are highly accurate, backed by 95-99% sensitivity and 95-100% specificity for fetal genotype differentiation in carrier mothers.
Your Investment in Certainty and Proactive Care
Knowing your baby’s status early is a profound investment. It is the beginning of a proactive care plan that can dramatically improve your child’s health outcomes.
The Fee for the SickleClear™ NIPT Screening is N850,000.
This single, all-inclusive fee covers the entire high-fidelity process:
- Specialized DNA blood collection tubes and logistics.
- Complex laboratory analysis in an ISO 15189–accredited genetics laboratory.
- Targeted HbS detection and rigorous internal/external quality checks.
- Expert bioinformatics processing and final report with clinical interpretation and next-step guidance.
Don’t leave the most important question to chance or delay. Gain the certainty you need today.