Peripheral Arterial Disease Trial, Recruiting NCT05624125 Sponsor: Northwestern University Condition: Peripheral Arterial Disease
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Peripheral Arterial Disease Trial, Recruiting

NCT05624125
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 50 years or older.
  • People who have been diagnosed with peripheral artery disease (PAD), a condition where blood flow to the legs is reduced, confirmed through specific circulation tests or imaging showing significant artery narrowing.
  • People whose circulation test results fall within a borderline range and show a notable drop in blood flow after a heel-rise exercise test.

Who may not be able to join:

  • People who have had an amputation of part or all of either leg.
  • People with severely reduced blood flow to the legs causing pain even at rest (a serious stage of PAD called critical limb ischemia).
  • People who use a wheelchair full-time or need a walker to get around.
  • People whose walking ability is limited by a condition other than PAD.
  • People who currently have an open sore or ulcer on the bottom of a foot.
  • People who do not complete the required study preparation period (the "run-in" phase).
  • People who have major surgery, heart procedures, or leg artery procedures planned within the next five months.
  • People who have had major surgery, heart procedures, leg artery procedures, or a serious heart event in the past three months.
  • People with serious medical conditions such as lung disease requiring oxygen use during the day, Parkinson's disease, a life-threatening illness with a life expectancy of less than six months, or cancer that has required treatment in the past two years. (People treated for an early-stage cancer with an excellent outlook, or those who only need oxygen at night, may still be considered — confirm with trial site.)
  • People who score below a certain threshold on a standard memory and thinking assessment (confirm with trial site).
  • People with an allergy to beetroot juice.
  • People who are currently consuming beetroot juice, beet supplements, or oral nitrate or nitrite products and who are not willing to stop taking them for 30 days before the study begins and throughout the trial.
  • People who currently eat one cup or more of beets daily and are not willing to reduce this for 30 days before the study begins and throughout the trial.
  • People who do not speak English.
  • People who have taken part in or completed another clinical trial in the past three months. (Different timeframes may apply depending on the type of trial previously completed — confirm with trial site.)
  • People whose vision problems affect their ability to walk.
  • People whose walking distance in a six-minute walking test falls below 500 feet or above 1,600 feet. (The trial team may use their judgement for those who walk more than 1,600 feet — confirm with trial site.)
  • People whose resting blood pressure is below 100/45.
  • People who have taken part in a supervised treadmill exercise program in the past three months.
  • People who currently use an antibacterial mouthwash (such as one containing chlorhexidine) and are not willing to stop using it.
  • People with significantly reduced kidney function or elevated potassium levels in their blood (confirm specific values with trial site).
  • People with a history of kidney stones that requires them to limit foods containing oxalate (a substance found in beetroot).
  • People whom the trial investigators determine, based on their clinical judgement, are not suitable or safe candidates for the trial.

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 14 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

Phone: 312-503-6419

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
Registry
ClinicalTrials.gov
Start date
25 January 2023
Est. completion
1 April 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Four-month change in six-minute walk distance

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: 14 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