Metformin BenefIts Lower Extremities With Intermittent Claudication (MOBILE_IC)

Who is this study for? Patients with Intermittent Claudication
What treatments are being studied? Metformin
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 35
Maximum Age: 89
Healthy Volunteers: f
View:

• 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)

• a. Participants may not comply with the above measures to meet inclusion criteria, but investigator driven attempts to maximize the optimal medical therapy, as tolerated, for each participant prior to trial enrollment

• 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)

Locations
United States
Pennsylvania
VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA
RECRUITING
Pittsburgh
Contact Information
Primary
Edith I Tzeng, MD
Edith.Tzeng@va.gov
(412) 360-1657
Backup
Katherine M Reitz
reitzkm2@upmc.edu
(412) 688-6000
Time Frame
Start Date: 2022-03-01
Estimated Completion Date: 2031-02-28
Participants
Target number of participants: 200
Treatments
Experimental: Metformin ER 1000mg
daily by mouth
Placebo_comparator: Matching placebo
daily by mouth
Sponsors
Collaborators: San Francisco Veterans Affairs Medical Center, Northwestern University, University of Pittsburgh
Leads: VA Office of Research and Development

This content was sourced from clinicaltrials.gov