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Not yet recruitingNCT06808607Updated Feb 5, 2025

Clinical Outcomes of Primary Versus Secondary Antiphospholipid Syndrome

An observational study in Antiphospholipid Syndrome, sponsored by Assiut University. Not yet recruiting at 1 site in Egypt. Open to participants aged 18 Years to 55 Years. Per ClinicalTrials.gov, last updated 2025-02-05.

Sponsored by Assiut University · Observational

From the registry’s dates

  • Primary completion was expected by Mar 2026, 7 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
52
Ages
18 Years to 55 Years
Sex
All
01

Study summary

Observational retrospective cohort study to assess clinical outcomes in patients with primary versus secondary antiphospholipid syndrome

Read the detailed description

Antiphospholipid antibody syndrome is an autoimmune disorder associated with positive antiphospholipid antibodies including the lupus anticoagulant, anticardiolipin antibodies IgG or IgM, and/or anti-ß2-glycoprotein IgG or IgM associated with thrombotic problems and pregnancy loss.

Antiphospholipid syndrome is one of the most frequent forms of acquired thrombophilia and is associated with an increased risk of both venous and arterial thrombotic events. Thirty to 40% of systemic lupus erythematosus (SLE) patients have associated antiphospholipid syndrome.

Antiphospholipid syndrome has estimated incidence in the general population of 2.1 (1.4-2.8) per 100 000, and the prevalence of 50 (42-58) per 100 000. APS is more common in female with a female to male ratio is 3.5:1 for primary and 7:1 for secondary.

Antiphospholipid syndrome is divided into two types primary syndrome without an underlying disease, and secondary antiphospholipid syndrome that is associated with another autoimmune syndrome, most commonly Systemic Lupus Erythematosus (SLE).

Patients with APS are more at risk of recurrent thrombosis (3). n a retrospective analysis of 160 patients with APS, venous thromboembolism (VTE) was found to be the commonest manifestation (47.5%) followed by arterial thromboembolism (43.1%) then materno fetal problems which were found only in 9.7% of patients, and finally, catastrophic antiphospholipid syndrome (CAPS) represented in only 2.5 percent of the cases (4).

The clinical manifestations of antiphospholipid syndrome include haematological (thrombocytopenia, venous thrombosis), obstetrical (recurrent pregnancy loss), neurological (stroke, transient ischaemic attack, seizures), cardiovascular, dermatological such as livedo reticularis, skin ulceration and necrosis, renal (glomerulonephritis and renal thrombotic microangiopathy), and orthopedic (avascular necrosis of bones).

the manifestation spectrum ranged from asymptomatic antiphospholipid antibodies positivity, various non-criteria manifestations, obstetric morbidity, thrombosis, to life-threatening catastrophic antiphospholipid syndrome. The wide manifestation spectrum led to a heterogeneous entity and brought challenges to management of the syndrome.

The aim of this study was to compare primary versus secondary effects of antiphospholipid syndrome on the development of thrombosis and its outcomes.

02

Conditions studied

  • Antiphospholipid Syndrome

Keywords

  • Thrombosis
  • Antiphospholipid syndrome
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In context

Antiphospholipid Syndrome

125 studies on the registry are indexed under Antiphospholipid Syndrome; 55 are open to participants now.

This study's planned enrollment of 52 is below the median of 161 across 53 observational studies indexed under Antiphospholipid Syndrome.

Browse Antiphospholipid Syndrome studies →

Lead sponsor

Assiut University is the lead sponsor of 5,050 studies on the registry; 2,174 are open to participants now.

Of its 14 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Retrospective cohort

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • All patients diagnosed as antiphospholipid syndrome in clinical hematology or rheumatology units in internal medicine department, Assiut university hospital.

Exclusion criteria

Exclusion Criteria:

  • patients with other risk factor for thrombosis (malignancy, cocs, protein c or protein s deficiency etc
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
52 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • Retrospective to compare clinical outcomes of primary versus secondary antiphospholipi

    Observational study to compare clinical outcomes of primary versus secondary antiphospholipid syndrome

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What researchers measure

Primary outcomes

  1. to compare percentage of patients with primary versus secondary antiphospholipid syndrome in developing recurrent thrombosis

    Time frame: 12 months

07

Study locations

1 site
  • Maha Abdel-Aziz
    Asyut, 71515, Egypt
08

References and documents

Individual participant data

Plan to share: Undecided — Undecided yet

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 5, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06808607
Lead sponsor
Assiut University
Responsible party
Maha Mohammed Abdel-Aziz (Lecturer of Clinical Hematology, Faculty of medicine, Assiut university, Assiut University) — Principal investigator
First posted
Feb 5, 2025
Start date
Feb 7, 2025 (estimated)
Primary completion
Mar 6, 2026 (estimated)
Completion
Mar 6, 2026 (estimated)
Last update
Feb 5, 2025

Study contacts

Maha Abdel-Aziz, Clinical Hematology MD
Contact
maha.hematology@aun.edu.eg
2001097278659
Yomna Refaat, Clinical Hematology MD
Contact
yomnarefaat@aun.edu.eg
+20 10 60178482

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jan 2025. You cannot join it, but the record below documents what was studied.

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