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Recruiting Observational

Hematological Markers MPV, PLR, and NLR in Primary Versus Secondary Antiphospholipid Syndrome

NCT07142239 · tracked via the Priya Life Science Egypt tracker
Phase
Observational
Started
2025-11-27
Last updated
2026-07-31

Condition(s) studied

Antiphospholipid Syndrome

Investigational drug(s) / intervention(s)

• Complete blood count , MPVCalculation of PLR: Platelet count / Lymphocyte count and Calculation of NLR:Antiphospholipid antibody profile

• Complete blood count , MPV: CBC report

Calculation of PLR: Platelet count / Lymphocyte count and Calculation of NLR:: CBC report

Antiphospholipid antibody profile: Patient record

Study summary

Antiphospholipid syndrome is a thrombo-inflammatory autoimmune disorder with a complex antiphospholipid antibody-mediated pathogenesis, and high heterogeneity in clinical presentation and disease course. Clinical presentation in antiphospholipid syndrome includes venous and arterial thrombosis, pregnancy complications, and a broad range of microvascular and non-thrombotic manifestations

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults (age ≥18 years) * Diagnosis of APS based on updated Sydney classification criteria confirmed by: Clinical history of thrombosis and/or pregnancy morbidity, Persistent presence (≥12 weeks) of antiphospholipid antibodies (aCL, anti-β2-glycoprotein I, and/or lupus anticoagulant) Exclusion criteria: * Current infection or inflammatory condition unrelated to APS * Hematological malignancies or other blood disorders * Recent blood transfusion or platelet-altering medications other than APS treatments

Primary outcome measure(s)

  • Measurement of Mean platelet Volume in patients diagnosed with primary APS — Baseline
  • Measurement of Mean platelet Volume in patients diagnosed with secondary APS — Baseline

Trial sites (1)

FacilityCityRegionStatus
New Valley University Al Khārjah Kharga Oasis Recruiting
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 NCT07142239 on ClinicalTrials.gov ↗ ← All trials in Egypt