Clinical Trials in the USA / NCT06690099
Active, not recruiting
Observational
Prospective Collection of Whole Blood Specimens From RhD Negative Pregnant Women
NCT06690099 · tracked via the Priya Life Science USA tracker
Condition(s) studied
Rhesus D GenotypePregnancy
Study summary
The purpose of this research is to collect blood samples and data from pregnant women who are Rh negative. The blood will be used for the future research and the development of non-invasive prenatal tests to identify Rh blood type status of the baby during pregnancy.
Eligibility
Inclusion Criteria:
1. Willing and able to provide written informed consent
2. 18 years of age or older at enrollment
3. Women with a viable pregnancy (with documented fetal heartbeat) between 12 weeks, 0 days and 28 weeks, 0 days gestational age
4. Women with RhD negative antigen status by serology
5. Willing to provide neonatal ABO and RhD genotyping status
Exclusion Criteria:
1\. Women with multiple gestation pregnancy
Primary outcome measure(s)
- Fetal RhD determination from maternal whole blood — 18 months
Collected samples will be used for future development of non-invasive prenatal test to determine fetal RhD status from maternal whole blood
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Ochsner Health | New Orleans | Louisiana |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06690099 on ClinicalTrials.gov ↗ ← All trials in the USA