Peripheral Arterial Disease Trial, Recruiting NCT07500610 Sponsor: Cardiology Research UBC Condition: Peripheral Arterial Disease
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Peripheral Arterial Disease Trial, Recruiting

NCT07500610
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People aged 19 years or older
  • People who are able to give informed consent before any trial activities begin
  • People who have been diagnosed with peripheral artery disease (PAD) causing leg pain or cramping when walking, at a stage where they can walk more than 200 metres (about 2 blocks) before needing to stop, and have had these stable symptoms for at least 90 days before the screening appointment
  • People whose PAD has been confirmed by a specific test result — either a low ankle-to-arm blood pressure comparison score (0.90 or below), or a significant narrowing in a leg artery shown by imaging tests, or a history of a procedure to restore blood flow in the legs

Who may not be able to join:

  • People who have used any medication that affects the immune system within the 90 days before screening
  • People whose ability to walk is limited by a condition other than PAD
  • People who have a leg orthopaedic surgery or other major surgery that affects walking ability planned at the time of screening
  • People who had a procedure to restore blood flow in leg arteries within the 180 days before screening
  • People who have an arterial blood flow procedure planned at the time of screening
  • People who have had a heart attack, stroke, hospitalisation for severe chest pain, or a mini-stroke within the 180 days before screening
  • People with heart failure that causes significant symptoms even with minimal activity or at rest (confirm with trial site)
  • People who have signs of severe reduced blood flow to the legs, such as gangrene, pain at rest, or wounds that are not healing

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 9 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Christopher Fordyce, MD MHS MSc FRCPC, Vancouver General Hospital

Phone: 604 875-5324

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Cardiology Research UBC
Registry
ClinicalTrials.gov
Start date
25 September 2025
Est. completion
30 April 2026

Where this trial is recruiting

🇨🇦 Canada

Primary endpoints

6-Minute Walk Test (6MWT)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 9 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov