Phase 4 Peripheral Arterial Disease Trial, Recruiting
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 who have a long-term history of claudication (leg pain or cramping during walking caused by reduced blood flow).
- People whose leg pain during walking has been confirmed by a vascular surgeon, both through discussion and by observing them during a walking test.
- People who have been found to have reduced blood flow in the arteries of their legs, confirmed through blood pressure measurements at the ankle compared to the arm, and/or other imaging tests.
- People who have had a stable, unchanged treatment routine for blood pressure, cholesterol, and diabetes (if applicable) for at least 6 weeks.
Who may not be able to join:
- People who have leg pain at rest or open sores or tissue damage on their legs caused by poor blood flow (sometimes called Fontaine stage III or IV disease).
- People who have recently had a sudden loss of blood flow to a leg caused by a blood clot or a physical injury.
- People whose ability to walk is significantly limited by conditions other than leg artery disease, such as joint or muscle problems, nerve problems, or heart or lung conditions.
- People who are currently taking a type of blood pressure medication called an ACE inhibitor or an angiotensin II receptor blocker.
- People who have chronic kidney disease with significantly reduced kidney function (a specific kidney filtration measurement below 30 ml/min/1.73m² — confirm with trial site if unsure how this applies).
- People who have a history of severe narrowing of the arteries supplying both kidneys.
- People who have previously had a serious allergic reaction called angioedema related to an ACE inhibitor medication, or who have a known allergy or sensitivity to ramipril or similar medications.
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.
Contact this trial
Principal Investigator: Iraklis I Pipinos, MD, University of Nebraska
Phone: 402-995-4171
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
Where this trial is recruiting
Primary endpoints
Absolute Claudication Distance
Can't join this trial?
Data last synced from ClinicalTrials.gov: 13 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.