ClinicalTrials.gg
RecruitingNCT07500610PANACEA-OUpdated Mar 30, 2026

Observing the Role of Inflammation in Peripheral Artery Disease and Its Impact on Heart and Mobility Health: PANACEA-O.

An observational study in Peripheral Vascular Disease, sponsored by Cardiology Research UBC. Recruiting at 1 site in Canada. Open to participants aged 19 Years and older. Per ClinicalTrials.gov, last updated 2026-03-30.

Sponsored by Cardiology Research UBC · Observational

From the registry’s dates

  • Primary completion was expected by Apr 2026, 6 months ago, but the record still lists the study as recruiting.
  • Started Sep 2025; still recruiting 1 year 1 month later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
50
Ages
19 Years and older
Sex
All
01

Study summary

This registry aims to collect detailed information about people in Canada who have Peripheral Artery Disease (PAD) and are receiving care in heart clinics while still able to walk and live in the community. Researchers want to better understand what these patients are like at the start of their care and looking at their general health, levels of inflammation in their bodies, and how well they can move and function in daily life.

The results of this study will help healthcare providers better understand what PAD looks like in today's Canadian heart clinics. It will also help guide future research studies that focus on inflammation and PAD. The researchers believe that PAD patients can be routinely recruited from these clinics, and that most of these patients will have high levels of inflammation (shown by high blood CRP levels) and poor physical ability when they first join. The findings will show that there is a strong need to regularly check for PAD in heart clinics so that patients can be identified early and offered new treatments in the future and especially treatments that may help reduce inflammation.

Read the detailed description

Peripheral arterial disease is a common manifestation of atherosclerosis that can lead to significant morbidity and mortality. Inflammation plays a key role in the pathogenesis of PAD. Although the pathophysiology of intermittent claudication is attributed primarily to a flow-limiting stenosis or occlusion of a conduit artery that limits oxygen delivery during exercise, a large body of evidence indicates that, with exercise, limb ischemia evokes an acute systemic response characterized by increased oxidative stress, inflammation, and endothelial dysfunction and guidelines recommend smoking cessation and supervised exercise therapy to improve IC, but there are few pharmacologic options.

Cilastozol, a selective and potent phosphodiesterase (PDE) 3A inhibitor and naftidrofuryl, a selective inhibitor of the 5-hydroxytryptamine (serotonin) receptor type 2 (5-HT2), both provide modest benefits on maximum walk distance.(3) However, methodologic inconsistencies, lack of hard objective endpoints, and multiple sources of potential bias in the cited studies supporting their approval have resulted in limited availability and uptake of these agents. While the upcoming STRIDE trial will evaluate the role of semaglutide in improving functional capacity in patients with T2D and PAD, additional strategies need to be evaluated.

The prevalence of PAD in an ambulatory population of patients at risk for this condition is unknown. There currently exists no registry (local or regional) that routinely documents this condition. There are some contemporary registries that exist, but this is mainly among patients with PAD who have already received a revascularization procedure. Furthermore, the prevalence of PAD, inflammation, and functional status is unknown.

The specific aims of this registry are to (1) capture the detailed patient demographic and prevalence of inflammation (i.e., CRP) among PAD patients in an ambulatory population of patients followed in Canadian cardiovascular clinics and (2) determine baseline functional capacity in these PAD patients at baseline with a 6- minute walk distance. The results of this prospective registry can help inform both the landscape of PAD in contemporary Canadian cardiovascular clinics as well as to inform enrollment of future clinical trials in this space targeting inflammation and PAD (i.e., PANACEA). It is hypothesized that PAD patients can be routinely recruited in cardiovascular clinics in Canada, with the vast majority having elevated CRP and relatively poor functional capacity at baseline. The results of this registry will demonstrate the unmet need to routinely screen and identify PAD patients within cardiovascular for future therapies that may be particularly helpful in this population, including those potentially targeting inflammation

The results of this registry have the potential to significantly impact clinical practice guidelines for the management of PAD. By providing robust data on the prevalence of inflammation and its correlation with functional impairment in PAD patients, this registry will underscore the importance of routine screening for PAD in cardiovascular clinics. The identification of patients with elevated CRP and poor functional capacity at baseline will highlight the need for early and targeted interventions, potentially leading to the development of new therapeutic strategies aimed at reducing inflammation and improving outcomes in this high-risk population. Additionally, the registry data may inform the design and enrollment of future clinical trials, contributing to the advancement of evidence-based practices in the management of PAD.

02

Conditions studied

  • Peripheral Vascular Disease

Keywords

  • peripheral vascular disease
  • inflammation
  • CRP
  • claudication
  • ABI
03

In context

Peripheral Vascular Diseases

443 studies on the registry are indexed under Peripheral Vascular Diseases; 44 are open to participants now.

This study's planned enrollment of 50 is below the median of 217 across 86 observational studies indexed under Peripheral Vascular Diseases.

Browse Peripheral Vascular Diseases studies →

Lead sponsor

Cardiology Research UBC is the lead sponsor of 18 studies on the registry; 7 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

PAD patients recruited from Cardiovascular Clinics at Vancouver General Hospital and McGill University Health Centre

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age >/= 19 years of age
  • Ability to provide before any trial-related activities
  • Symptomatic PAD with intermittent claudication corresponding to Fontaine stage IIa meeting all of the following:

    1. Stable symptoms of PAD with intermittent claudication in Fontaine stage IIa (able to walk without stopping more than 200 m/656 feet/2 blocks) for at least 90 days prior to the day of screening based on patient interview.
    2. Ankle-brachial-index (ABI) equal to or below 0.90 (the leg with lowest index is chosen in case of bilateral disease) or ≥ 50% stenosis in peripheral artery (excluding carotid) documented by X-ray angiography, MR angiography, CT angiography or Doppler ultrasound, or a history of lower extremity revascularization

Exclusion criteria

Exclusion Criteria:

  • Current or previous treatment with any immunomodulating agent within 90 days prior to the day of screening.
  • Walking ability limited by conditions other than PAD
  • Planned orthopaedic surgery in the legs, or other major surgery known on the day of screening (surgery affecting walking ability).
  • Vascular revascularisation procedure for PAD of any kind 180 days prior to the day of screening.
  • Planned arterial revascularisation known on the day of screening.
  • Myocardial infarction, stroke, hospitalisation for unstable angina pectoris or within 180 days prior to the day of screening.
  • Heart failure presently classified as being in (NYHA) class III-IV.
  • Signs/symptoms of critical limb ischemia (leg gangrene, rest pain, ischemic wounds, etc)
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

TIA (transient ischaemic attack)

A “mini-stroke”: temporary stroke-like symptoms caused by reduced blood flow to part of the brain, spinal cord or eye, without signs of a new stroke on a scan.

Stroke symptoms need emergency care at once, even if they go away.

NYHA class (heart failure)

The New York Heart Association’s four classes of how much heart failure limits physical activity.

I
No limits: ordinary activity causes no undue tiredness or breathlessness.
II
Slight limits: comfortable at rest, ordinary activity causes symptoms.
III
Marked limits: comfortable at rest, less than ordinary activity causes symptoms.
IV
Symptoms even at rest; any activity makes them worse.

Studies set their own limit — many outside heart failure leave out class III–IV, while heart failure studies may ask for a particular class. Check the class this study names.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
50 participants (estimated)
Target follow-up
1 Day
Patient registry
Yes

Groups and cohorts

  • PAD
06

What researchers measure

Primary outcomes

  1. 6-Minute Walk Test (6MWT)

    Distance in metres walked in 6 minutes as a measure of functional capacity

    Time frame: Baseline visit

Secondary outcomes

  1. High-sensitivity C-reactive Protein (hs-CRP)

    Unit: mg/L

    Time frame: Baseline visit

  2. Left Ventricular Ejection Fraction (LVEF)

    Unit: %

    Time frame: Baseline visit

  3. VascuQoL-6 Total Score

    Vascular Quality of Life Questionnaire (VascuQoL-6): Each question is scored 1-4.

    Time frame: Baseline visit

  4. Systolic Blood Pressure

    Unit: mmHg

    Time frame: Baseline visit

  5. Heart Rate

    Unit: bpm

    Time frame: Baseline visit

07

Study locations

1 of 1 sites recruiting
  • Vancouver General Hospital
    Vancouver, British Columbia V5Z 1M9, Canada
    Recruiting
    • Jackie Chow, BSN · Contactjackie.chow@vch.ca · 604 875-5324
    • Bianca Marginean, BSc, MM · Contactbianca.marginean@ubc.ca · 604 875-4111
    • Christopher Fordyce, MD MHS MSc FRCPC · Principal investigator
    • Darryl Wan, MD, FRCPC, RPVI · Sub investigator
08

References and documents

Individual participant data

Plan to share: Yes — The registry data at the end of the registry may lead to the possible design of a larger trial (to calculate the sample size and build data collection instruments).The registry investigator will have access to the de-identified dataset after the end of the registry.

Supporting information: Clinical study report

Time frame: At the end of the registry for approximately one year.

Access criteria: The registry investigator will have access to the de-identified dataset after the end of the registry.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 30, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07500610
Lead sponsor
Cardiology Research UBC
Collaborators
Novo Nordisk A/S
Responsible party
Sponsor
First posted
Mar 30, 2026
Start date
Sep 25, 2025
Primary completion
Apr 30, 2026 (estimated)
Completion
Jul 2026 (estimated)
Last update
Mar 30, 2026

Study contacts

Jackie Chow, BSN
Contact
jackie.chow@vch.ca
604 875-5324
Robyn Szchory, BSN
Contact
robyn.szchory@ubc.ca
604 875-5120
Christopher Fordyce, MD MHS MSc FRCPC
principal investigator · Vancouver General Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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