Fisetin to Reduce Senescence and Mobility Impairment in PAD

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age50+
SponsorNorthwestern University

About this trial

The investigators propose a pilot randomized trial to gather preliminary data to test the hypothesis that Fisetin will reduce abundance of senescent cells in blood, skeletal muscle, and both subcutaneous and inter muscular adipose tissue and improve 6-minute walk distance in 34 people with peripheral artery disease (PAD). the investigators will determine whether greater declines in abundance of cells with senescent markers are associated with greater improvement in 6-minute walk distance in people with peripheral artery disease. In exploratory analyses, the investigators will assess whether Fisetin reduces interleukin-6 (IL-6) and novel senescent markers in adipose tissue, muscle, and/or blood.

Eligibility criteria

Qualifiers

An ankle brachial index (ABI) less than or equal to 0.90 at baseline.

Vascular lab evidence of PAD (such as a toe brachial pressure less than or equal to 0.70 or an ankle brachial index less than or equal to 0.90), or angiographic evidence of PAD defined as at least 70% stenosis of an artery supplying the lower extremities.

An ABI of greater than 0.90 and less than or equal to 1.00 who experience a 20% or greater drop in ABI in either leg after the heel-rise test will also be included.

Disqualifiers

Above- or below-knee amputation

Critical limb ischemia defined as an ABI less than 0.40 with signs or symptoms of critical limb ischemia

Wheelchair confinement or requiring a walker to ambulate

Walking is limited by a symptom other than PAD

Trial design

Treatments tested in this trial

  • Fisetin
  • Placebo

Treatment groups

34 Participants
are divided into 2 treatment groups

Sponsors and collaborators