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:
For the LEAD (leg artery disease) group:
- People who have been diagnosed with lower limb artery disease (a condition where reduced blood flow affects the legs)
- People experiencing symptoms ranging from no pain at rest through to severe limb pain or wounds, as classified by the Fontaine scale stages I through IV
For the comparison (control) group:
- People aged between 35 and 85 years
- People who have at least one of the following: high blood pressure, diabetes, heart artery disease, or who currently smoke
Who may not be able to join:
- People younger than 35 or older than 85 years
- People with a body mass index (BMI) of 40 or higher (confirm with trial site for exact calculation)
- People who have a history of heart failure
- People with any autoimmune or rheumatic disease (conditions where the immune system attacks the body, such as rheumatoid arthritis or lupus)
- People with a history of certain structural heart diseases, including inflammatory, infiltrative, or non-ischaemic heart muscle diseases
- People who have had a heart attack or acute heart event within the last 3 months
- People with moderate to severe heart valve disease
- People who have previously had surgery or a procedure to treat a heart valve
- People who have a device implanted in their heart, such as a pacemaker or defibrillator
- People who have had a mini-stroke (TIA) or stroke within the last 3 months
- People with severe chronic lung disease (classified as GOLD stage C or D)
- People with moderate to severe asthma (as defined by GINA 2022 guidelines)
- People with untreated high blood pressure measuring 180/110 mmHg or higher at the time of recruitment
- People with severely reduced kidney function (eGFR below 30 ml/min/1.73 m²)
- People who have received radiation to the chest area, or who have a history of cancer treatment including chemotherapy or biological therapies
- People with a chronic blood disorder (other than anaemia)
- People with severe liver disease
- People who have had a cancer diagnosis and have been in remission for less than 5 years
- People with an active or ongoing infectious disease
- People with anaemia where the haemoglobin level is below 80 g/L
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: Jaak Kals, PhD, Tartu University Hospital
Phone: 731 8292
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
left ventricular global longitudinal strain (GLS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.