Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
30 participants
OBSERVATIONAL
2025-07-17
2026-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Youngs
Patients aged 18 to 30 requiring coronary artery bypass grafting (CABG).
Graft collection
Sampling of superior venous and arterial grafts (internal mammary artery, great saphenous vein) after coronary artery bypass surgery.
Middle-aged
Patients aged 30 to 60 requiring coronary artery bypass grafting (CABG).
Graft collection
Sampling of superior venous and arterial grafts (internal mammary artery, great saphenous vein) after coronary artery bypass surgery.
Elderly
Patients aged 60 and more requiring coronary artery bypass grafting (CABG).
Graft collection
Sampling of superior venous and arterial grafts (internal mammary artery, great saphenous vein) after coronary artery bypass surgery.
Interventions
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Graft collection
Sampling of superior venous and arterial grafts (internal mammary artery, great saphenous vein) after coronary artery bypass surgery.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Centre Hospitalier Universitaire de Saint Etienne
OTHER
Responsible Party
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Principal Investigators
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Salvatore CAMPISI, MD
Role: PRINCIPAL_INVESTIGATOR
CHU SAINT-ETIENNE
Locations
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CHU Saint-Etienne
Saint-Etienne, France, France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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IRBN502025/CHUSTE
Identifier Type: -
Identifier Source: org_study_id
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