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NCT Number: NCT06626646

Vascular Regenerative Cell Exhaustion in Adults with Peripheral Artery Disease (PAD-VRCE)

PAD-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.

Recruiting

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

North York Diagnostic and Cardiac Centre, North York, Ontario, Canada

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About this study

Individuals with peripheral artery disease (PAD) have been shown to have poorer cardiovascular health outcomes than the general population. It is believed that the number of people living with PAD is greatly underestimated and furthermore, mortality due to the most severe form of PAD - critical limb ischemia - is increasing. There is a growing body of evidence that the presence of cardiovascular risk factors leads to the imbalance of circulating regenerative cells. The aggregate impact of this regenerative cell exhaustion phenotype is an increased risk of adverse events and progression of disease states.

PAD-VRCE is an observational, cross-sectional, two-arm cohort study aimed at determining the differences in the progenitor cell profiles in the blood of individuals with PAD in comparison to individuals without PAD. We hypothesize that people with PAD will exhibit depleted levels of these progenitor cells defined as vascular regenerative cell exhaustion. VRCE impacts the function of anti-inflammatory cells and associated repair mechanisms within blood vessels, and may contribute to the differential long term outcomes between the two groups.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults ≥18 and ≤80 years of age who meet either of the following criteria:
  • Clinically significant/symptomatic PAD (defined as symptomatic claudication with and an ankle brachial index of less than 0.85).
  • No history of PAD.
  • Willing and able to provide written informed consent and comply with study procedures.

Exclusion criteria

  • Unable or unwilling to provide written informed consent or to provide a peripheral blood sample.
  • Any life-threatening disease expected to result in death within two years.
  • 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.
  • Uncontrolled hypertension.
  • New York Heart Association Class IV heart failure.
  • Active liver disease or liver dysfunction.
  • Active kidney disease or kidney dysfunction.
  • History of hemorrhagic stroke or other major bleeding disorder.
  • White blood cell count of ≥15x10^9/L.
  • Active infectious disease requiring systemic antibiotic or anti-viral agents.
  • Known acquired immunodeficiency syndrome, such as Human Immunodeficiency Virus.
  • On oral steroid therapy (e.g. prednisone or other corticosteroids) or other immunosuppressive agents (e.g. methotrexate).
  • Treated autoimmune disorders

Treatment and study plan

Primary outcomes

  1. The difference in the frequency / absolute number of circulating primitive myeloid progenitor cells (ALDHhiSSClow) between individuals with PAD and without PAD

    Time frame: Baseline

Secondary outcomes

  1. The difference in the amount of intracellular reactive oxygen species produced by ALDHhi progenitor cell subsets in individuals with PAD and without PAD

    Time frame: Baseline

  2. The difference in the levels of circulating inflammatory and oxidative stress markers in individuals with PAD and without PAD

    Time frame: Baseline

  3. The difference in the frequency /absolute count of ALDHhiSSCmid monocytes in individuals with PAD or without PAD

    Time frame: Baseline

Study contacts

Contact information is provided by the study sponsor or research team.

Aishwarya Krishnaraj, BScH

CONTACT

[email protected]

Jack Casey

CONTACT

[email protected]

604-703-5449

Sponsors and collaborators

Lead sponsor

Canadian Medical and Surgical Knowledge Translation Research Group

Other

Registry information

Official study title

Vascular Regenerative Cell Exhaustion in Adults with Peripheral Artery Disease

Acronym: PAD-VRCE

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Oct 4, 2024
Registry last updated
Oct 4, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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