Measuring Tryptase Levels in Patients with Stable Coronary Artery Disease
Official title: Investigation of the Role and Prognostic Value of Tryptase in Patients With Stable Coronary Artery Disease
Run by University of Thessaly · NCT06958016 · Data updated 2026-11-12
This study is testing if measuring tryptase levels in people with stable coronary artery disease can help predict their risk of having serious heart problems in the future.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 85 Years |
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | University of Thessaly Academic / other |
| Locations | 2 sites (Athens, Attica and 1 other locations) |
| Status | Recruiting |
| Started | January 12, 2024 |
| Main results expected | January 11, 2026 |
| Study ends | January 11, 2027 |
| Registry record updated | May 28, 2025 |
| Trial ID | NCT06958016 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are males and females aged 18 to 85 with clinical symptoms of angina and a positive SPECT scan for myocardial ischemia.
✕Probably not a fit
Patients with acute coronary syndrome, recent coronary interventions, or certain medical conditions such as autoimmune diseases or cancer may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to measure serum tryptase levels in patients with stable coronary artery disease (CAD) and correlate these levels with the severity of their condition. It will investigate the potential of tryptase as a prognostic biomarker for predicting future cardiovascular events, particularly the transition from chronic coronary syndrome (CCS) to acute coronary syndrome (ACS). The study focuses on the role of mast cell activation in plaque instability, which may contribute to sudden cardiovascular events in patients with CCS. By analyzing the relationship between tryptase levels and cardiovascular health, the study seeks to enhance understanding of CAD progression.
Why it matters
Potential benefit: If successful, this study could provide a new biomarker for predicting cardiovascular events in patients with chronic coronary syndrome.
How similar studies have gone: Previous studies have indicated a potential link between tryptase levels and coronary artery disease, suggesting that this approach may yield valuable insights.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Male and female subjects aged 18 - 85 years old. * Clinical symptoms of angina which are classified based on the Canadian Cardiovascular Score (CCS score) * Positive SPECT scan for myocardial ischemia Exclusion Criteria: * Acute Coronary Syndrome 4 weeks before the coronary catheterization * Percutaneous Coronary Angioplasty * Coronary Artery Bypass Graft * Active symptoms of allergy (asthma, urticaria) * Mastocytosis * Hypereosinophilia * Autoimmune disease * Cancer * Kidney failure * Myelodysplastic Syndrome * Denial of signing informed consent
Where it's running
-
417 Military Hospital NIMTS
Athens, Attica, Greece Recruiting -
Larisa University Hospital
Larissa, Thessaly, Greece Recruiting
Study contacts
- Study coordinator: Fotios Skoufis, MD Medicine
- Email: fskoufis@hotmail.com
- Phone: +306981088650
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.