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NCT07209748

sCD163 in HELLP Syndrome

Sponsor: Assiut University

View on ClinicalTrials.gov

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).

Official title: The Significance of Soluble CD163 as a Novel Biomarker in the Early Detection and Severity Assessment of HELLP Syndrome

Key Details

Gender

FEMALE

Age Range

18 Years - 45 Years

Study Type

OBSERVATIONAL

Enrollment

70

Start Date

2025-12-01

Completion Date

2027-02

Last Updated

2025-10-07

Healthy Volunteers

Not specified

Interventions

DIAGNOSTIC_TEST

sCD163 level

The significance of soluble CD163 level in the early detection and severity assessment of HELLP Syndrome