Modality Choice Before and After Failure for the Treatment of Painful Diabetic Neuropathy
Sponsored by University of Michigan
About this study
The research team will perform a comparative-effectiveness sequential, multiple assignment, randomized trial in painful diabetic neuropathy (PDN) patients for 8 total months, divided into two 4-month stages. 600 participants 18+ with PDN will be enrolled in this study. The main goal is to compare the utility of three modalities (oral, topical, and behavioral) for initial PDN treatment, and to compare the utility of switching modalities versus continuing with the same modality for non-responders. Pain and discontinuation will be assessed weekly, whereas other outcomes will be assessed monthly for 8 months.
Where this study is enrolling (18)
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Stanford University
Stanford, California
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University of Florida-Jacksonville
Jacksonville, Florida
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Rush University Medical Center
Chicago, Illinois
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University of Iowa
Iowa City, Iowa
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University of Michigan
Ann Arbor, Michigan
Show all 18 locations
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Allina Health-Neurosciences Research
Minneapolis, Minnesota
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University of Minnesota
Minneapolis, Minnesota
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University of Missouri
Columbia, Missouri
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University of Nebraska
Omaha, Nebraska
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Will Cornell Medicine
New York, New York
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University of North Carolina
Chapel Hill, North Carolina
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Duke University
Durham, North Carolina
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Oregon Health & Science University
Portland, Oregon
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University of Pittsburgh
Titusville, Pennsylvania
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Meharry Medical College
Nashville, Tennessee
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BaylorScott & White University Medical Center
McKinney, Texas
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DHR Health Institute for Research and Development
Edinburg, Texas
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Essentia Health
Spooner, Wisconsin
Who can participate
Inclusion criteria
- ✓Diabetes
- ✓Painful Diabetic Neuropathy (confirmed at screening visit)
- ✓Willing to accept random treatment assignment to any of the proposed interventions
Exclusion criteria
- ✕Pregnancy or plans to become pregnant during the study
- ✕History of neuropathy from causes other than diabetes as determined through medical and family history, physical and neurologic examinations
- ✕HbA1c \>10%
- ✕Participation in an experimental medication trial within 3 months of starting the study
- ✕Undergoing therapy for malignant disease other than basal-cell or squamous-cell skin cancer
- ✕Medical or psychiatric reason for not being a study candidate according to the site PI's discretion
- ✕Contraindications preventing trialing two interventions within any of the 3 modalities
- ✕Cirrhosis of the liver
Only the research team can confirm whether you qualify. The intake questionnaire is the best way to find out.
Completing a questionnaire on Clinably does not enroll you in a clinical trial or confirm your eligibility. Only the research team can determine whether you qualify to participate. These results are based on the information you provide and are intended to help you start a conversation with the research team.
Trial data sourced from ClinicalTrials.gov.