MetfOrmin BenefIts Lower Extremities With Intermittent Claudication

Description

Peripheral arterial disease (PAD) affects over 20% of aged adults and is very common among Veterans due significant tobacco use. PAD is due to the progressive blockage of peripheral arteries, predominantly to the legs, and results in intermittent claudication (IC) or recurrent muscle pain with activity secondary to insufficient blood supply. Those with PAD and IC experience a progressive decline in walking and poor quality of life. There is no effective medical treatment for PAD and IC. Metformin is a safe and effective treatment for Type 2 diabetes but it can also reduce inflammation, oxidative stress, and improve energy requirements as well as improve blood flow to the legs. Therefore, the investigators will test the ability of Metformin to improve overall functional status, reduce PAD progression, and reduce systemic inflammation in Veterans suffering from PAD and IC in a randomized, placebo controlled trial: Metformin BenefIts Lower Extremities with Intermittent Claudication (MOBILE IC) Trial. The success of this trial may identify a safe and effective treatment for PAD and IC.

Conditions

Intermittent Claudication

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Study Overview

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Study Details

Study overview

Peripheral arterial disease (PAD) affects over 20% of aged adults and is very common among Veterans due significant tobacco use. PAD is due to the progressive blockage of peripheral arteries, predominantly to the legs, and results in intermittent claudication (IC) or recurrent muscle pain with activity secondary to insufficient blood supply. Those with PAD and IC experience a progressive decline in walking and poor quality of life. There is no effective medical treatment for PAD and IC. Metformin is a safe and effective treatment for Type 2 diabetes but it can also reduce inflammation, oxidative stress, and improve energy requirements as well as improve blood flow to the legs. Therefore, the investigators will test the ability of Metformin to improve overall functional status, reduce PAD progression, and reduce systemic inflammation in Veterans suffering from PAD and IC in a randomized, placebo controlled trial: Metformin BenefIts Lower Extremities with Intermittent Claudication (MOBILE IC) Trial. The success of this trial may identify a safe and effective treatment for PAD and IC.

Metformin BenefIts Lower Extremities With Intermittent Claudication (MOBILE_IC)

MetfOrmin BenefIts Lower Extremities With Intermittent Claudication

Condition
Intermittent Claudication
Intervention / Treatment

-

Contacts and Locations

Pittsburgh

VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA, Pittsburgh, Pennsylvania, United States, 15240

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Male and Female Veteran \>35 \& \<89
  • * Symptoms of Intermittent claudication
  • * Medically stable, optimal medical therapy (for \>3 months prior to randomization which includes - statin and anti-platelet therapy, blood pressure control, smoking cessation and physical activity counseling)
  • * PAD as defined by ABI \<0.9 or \>0.9 with evidence of PAD as documented by pulse volume recordings (within 6 months prior to expected randomization date)
  • * Maximum Walking Distance (MWD) on the 6-minute walk test (6MWT) of greater than or equal to 50 meters with onset of pain before or at 400 meters without the use of a walker (cane is acceptable; within 6 months of expected randomization date)
  • * Diabetes (Type I or II) or Hemoglobin A1c\>6.5 (within 6 months of expected randomization)
  • * Currently Taking metformin or have previously taken metformin (within 6 months of enrollment)
  • * Medical condition that limit their ability to ambulate other than PAD (i.e., Angina, CHF, pulmonary disease requiring oxygen, malignancy requiring treatment, etc.)
  • * Prior above or below knee amputation
  • * Critical limb threatening ischemia (i.e., non-healing wounds or rest pain)
  • * Planned hospital admission, major operation, or lower extremity revascularization to be completed (within 12 months after expected randomization date)
  • * Prior major operation or lower extremity revascularization (within the 3 months before expected randomization)
  • * Unable to complete quality of life testing due to Non-English Speaking and/or Dementia
  • * Kidney disease - dialysis or eGFR\<45 (within 6 months of expected randomization date)\*
  • * Planned iodinated contrasted study (within 6 months of expected randomization date)
  • * Evidence current or history of hepatic failure
  • * Women who are pregnant or breast feeding
  • * Unable to swallow uncrushed pills
  • * Investigator expects inclusion could cause harm to subject

Ages Eligible for Study

35 Years to 89 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

VA Office of Research and Development,

Edith I. Tzeng, MD, PRINCIPAL_INVESTIGATOR, VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA

Study Record Dates

2031-02-28