CSP #2001 - Investigation of Rifampin to Reduce Pedal Amputations for Osteomyelitis in Diabetics (VA Intrepid)

Who is this study for? Adult patients with Osteomyelitis
What treatments are being studied? Rifampin
Status: Active_not_recruiting
Location: See all (30) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

The purpose of this research study is to determine if rifampin, an antibiotic (a medicine that treats infections), is effective in treating osteomyelitis (infection of the bone) of the foot in diabetic patients. Despite use of powerful antibiotics prescribed over a long period of time, many diabetic patients remain at a high risk for needing an amputation of part of the foot or lower leg because the osteomyelitis is not cured. Some small research studies have shown that addition of rifampin to other antibiotics is effective in treating osteomyelitis in both diabetics and non-diabetics. However, because few diabetics with osteomyelitis have been studied, there is no definite proof that it is better than the usual treatments for diabetic patients. If this study finds that adding rifampin to the usual antibiotics prescribed for osteomyelitis reduces the risk for amputations, doctors will be able to more effectively treat many Veteran patients with this serious infection. Improving treatment outcomes is an important healthcare goal of the VA.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 89
Healthy Volunteers: f
View:

• Age 18 and 89 years

• Diagnosis of diabetes mellitus, either by: 1) use of oral hypoglycemic agents or insulin at the time of enrollment; 2) a hemoglobin A1c (HgA1c) level within the past 90 days \> 6.5; or 3) a medical record diagnosis of diabetes mellitus by a clinician on two or more occasions in the previous 10 years

• Definite or probable osteomyelitis in the diabetic foot, as defined by the International Working Group on the Diabetic Foot (Table 1). Criteria must be present at some point within 90 days prior to enrollment.

• All planned debridement has been completed prior to randomization.

• A course of backbone antimicrobial therapy has been selected.

Locations
United States
Arizona
Phoenix VA Health Care System, Phoenix, AZ
Phoenix
California
VA Loma Linda Healthcare System, Loma Linda, CA
Loma Linda
VA Long Beach Healthcare System, Long Beach, CA
Long Beach
VA Palo Alto Health Care System, Palo Alto, CA
Palo Alto
VA Northern California Health Care System, Mather, CA
Sacramento
VA Greater Los Angeles Healthcare System, West Los Angeles, CA
West Los Angeles
Colorado
Rocky Mountain Regional VA Medical Center, Aurora, CO
Aurora
Washington, D.c.
Washington DC VA Medical Center, Washington, DC
Washington D.c.
Florida
Bay Pines VA Healthcare System, Pay Pines, FL
Bay Pines
North Florida/South Georgia Veterans Health System, Gainesville, FL
Gainesville
Miami VA Healthcare System, Miami, FL
Miami
James A. Haley Veterans' Hospital, Tampa, FL
Tampa
Georgia
Atlanta VA Medical and Rehab Center, Decatur, GA
Decatur
Michigan
VA Ann Arbor Healthcare System, Ann Arbor, MI
Ann Arbor
Minnesota
Minneapolis VA Health Care System, Minneapolis, MN
Minneapolis
Missouri
St. Louis VA Medical Center John Cochran Division, St. Louis, MO
St Louis
North Carolina
Salisbury W.G. (Bill) Hefner VA Medical Center, Salisbury, NC
Salisbury
New York
James J. Peters VA Medical Center, Bronx, NY
The Bronx
Ohio
Cincinnati VA Medical Center, Cincinnati, OH
Cincinnati
Louis Stokes VA Medical Center, Cleveland, OH
Cleveland
Dayton VA Medical Center, Dayton, OH
Dayton
Oklahoma
Oklahoma City VA Medical Center, Oklahoma City, OK
Oklahoma City
Oregon
VA Portland Health Care System, Portland, OR
Portland
Tennessee
Tennessee Valley Healthcare System Nashville Campus, Nashville, TN
Nashville
Texas
VA North Texas Health Care System Dallas VA Medical Center, Dallas, TX
Dallas
Michael E. DeBakey VA Medical Center, Houston, TX
Houston
South Texas Health Care System, San Antonio, TX
San Antonio
Utah
VA Salt Lake City Health Care System, Salt Lake City, UT
Salt Lake City
Virginia
Salem VA Medical Center, Salem, VA
Salem
Wisconsin
William S. Middleton Memorial Veterans Hospital, Madison, WI
Madison
Time Frame
Start Date: 2018-01-22
Completion Date: 2025-12-31
Participants
Target number of participants: 843
Treatments
Active_comparator: Active drug
Patients receive oral adjunctive rifampin therapy
Placebo_comparator: Placebo
Patients receive oral riboflavin
Related Therapeutic Areas
Sponsors
Leads: VA Office of Research and Development

This content was sourced from clinicaltrials.gov