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Clinical Trials in Turkey / NCT07034586
Active, not recruiting Observational

Prospective Evaluation of Adventitial Histopathology in Borderline Ascending Aortic Dilatatio

NCT07034586 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2023-08-01
Last updated
2025-06-24

Condition(s) studied

Ascending Aortic AneurysmAortic Adventitial PathologyCoronary Artery Bypass Grafting (CABG)Borderline Aortic Dilatation

Study summary

This prospective study investigates microscopic changes in the outer layer (adventitia) of the ascending aorta in patients undergoing coronary artery bypass grafting (CABG) surgery. The study includes two groups of patients: (1) those with borderline ascending aortic dilatation (4.0-5.0 cm), and (2) a control group with normal aortic diameter (\<4.0 cm), all undergoing the same surgical procedure. During CABG, a small circular punch is routinely made in the ascending aorta for the proximal saphenous vein graft anastomosis. The tissue removed from this punch site is collected and used for histopathological and immunohistochemical analysis. The study aims to determine whether adventitial changes correlate with aortic size and whether these changes can help identify patients at risk for future aortic dissection or rupture. The findings may guide surgical decision-making in patients with borderline aortic enlargement.

Eligibility

Sex
ALL
Min age
20 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: 1. Adults aged between 20 and 70 years 2. Patients scheduled for elective open-heart coronary artery bypass grafting (CABG) 3. Patients undergoing their first cardiac surgery 4. Metabolically stable patients 5. Aortic diameter: 1. Observational aortic dilatation group: between 4.0 cm and 5.0 cm 2. Control group: less than 4.0 cm 6. Written informed consent obtained from the patient Exclusion Criteria: 1. History of previous cardiac surgery 2. History of aortic dissection or rupture 3. Known genetic syndromes (e.g., Marfan, Loeys-Dietz, Ehlers-Danlos) 4. Known systemic vasculitis 5. Presence of acute infection or systemic inflammatory disease 6. Inadequate biopsy material for pathological analysis 7. Patients not undergoing any aortic intervention during surgery

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Samsun University Faculty of Medicine Samsun Turkey (Türkiye)

More Samsun University trials in Turkey

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 NCT07034586 on ClinicalTrials.gov ↗ ← All trials in Turkey