Clinical Trial

sCD163 in HELLP Syndrome

Not Yet Recruiting
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Summary
Primary Aim: \_To investigate the diagnostic potential of soluble CD163 (sCD163)as a novel biomarker for the early detection of HELLP syndrome, assessing its sensitivity and specificity compared to current diagnostic markers. Secondary Aims: 1. To evaluate the correlation between sCD163 levels and the clinical severity of HELLP syndrome, including complications such as liver dysfunction, thrombocytopenia, and hemolysis. 2. To compare sCD163 levels across different stages of HELLP syndrome (partial vs. complete and other hypertensive disorders of pregnancy (e.g., preeclampsia).
Trial Details
NCT Number NCT07209748
Lead Sponsor Assiut University
Conditions HELLP Syndrome Complicating Pregnancy
Enrollment 70 participants
Start Date 2025-12-01
Primary Completion 2026-12 (estimated)
Study Completion 2027-02 (estimated)
Updated on ClinicalTrials.gov 2025-10-07