Vascular Regenerative Cell Exhaustion in Adults with Peripheral Artery Disease (PAD-VRCE)
Cardiovascular Disease | Type 2 Diabetes | Peripheral Artery Disease | Peripheral Vascular DiseasesPAD-VRCE is an observational, cross-sectional, two arm study aimed at determining if the presence of peripheral artery disease (PAD) can influence the number of circulating regenerative cells in blood. From peripheral blood samples, circulating progenitor cell content will be assessed via flow cytometry and compared between individuals with PAD and individuals without PAD. Ultimately, this study plans to evaluate the relationship between PAD, vascular regenerative cell exhaustion and overall cardiovascular health.
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Participation Requirements
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Sex:
ALL -
Eligible Ages:
18 to 80
Participation Criteria
Inclusion Criteria:
1. Adults ≥18 and ≤80 years of age who meet either of the following criteria:
1. Clinically significant/symptomatic PAD (defined as symptomatic claudication with and an ankle brachial index of less than 0.85).
2. No history of PAD.
2. Willing and able to provide written informed consent and comply with study procedures.
Exclusion Criteria:
1. Unable or unwilling to provide written informed consent or to provide a peripheral blood sample.
2. Any life-threatening disease expected to result in death within two years.
3. Any malignancy not considered cured (except basal cell carcinoma of the skin). An individual is considered cured if there has been no evidence of cancer recurrence for the five years prior to screening.
4. Uncontrolled hypertension.
5. New York Heart Association Class IV heart failure.
6. Active liver disease or liver dysfunction.
7. Active kidney disease or kidney dysfunction.
8. History of hemorrhagic stroke or other major bleeding disorder.
9. White blood cell count of ≥15x10\^9/L.
10. Active infectious disease requiring systemic antibiotic or anti-viral agents.
11. Known acquired immunodeficiency syndrome, such as Human Immunodeficiency Virus.
12. On oral steroid therapy (e.g. prednisone or other corticosteroids) or other immunosuppressive agents (e.g. methotrexate).
13. Treated autoimmune disorders
Study Location
Diagnostic Assessment Centre
Diagnostic Assessment CentreScarborough, Ontario
Canada
Contact Study Team
North York Diagnostic and Cardiac Centre
North York Diagnostic and Cardiac CentreNorth York, Ontario
Canada
Contact Study Team
- Study Sponsored By
- Canadian Medical and Surgical Knowledge Translation Research Group
- Participants Required
- More Information
- Study ID:
NCT06626646