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Orthotics
Orthotic Treatment for Diabetic Foot Ulcers
N/A
Recruiting
Led By Muturi G. Muriuki, PhD
Research Sponsored by VA Office of Research and Development
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Must not have
Veteran patients without palpable pedal pulse will be excluded
Veteran patients with a Meggitt-Wagner score of 4 or more will be excluded
Timeline
Screening 3 weeks
Treatment Varies
Follow Up at each clinic visit through study completion, an average of 8 months
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing a new way to heal diabetic foot ulcers that is faster and reduces the chance of the ulcer coming back.
Who is the study for?
This trial is for veteran patients with diabetic foot ulcers who are prescribed an orthotic walking boot. Participants must be able to understand instructions (with a BIMS score above 7), have palpable pedal pulses, and be ambulatory. Those with severe cognitive impairment, serious infections, amputations above the ankle, or very advanced ulcers (Meggitt-Wagner score of 4+) cannot join.
What is being tested?
The study is testing whether using a removable cam walker boot and providing counseling can reduce healing time for diabetic foot ulcers, prevent future ulcers, and improve quality of life compared to standard care alone in veterans.
What are the potential side effects?
Potential side effects may include skin irritation from the boot, discomfort while walking with the orthotic device, or stress due to adherence to treatment protocols. Counseling typically does not have physical side effects but can sometimes bring up emotional issues.
Eligibility Criteria
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am a veteran with a detectable pulse in my feet.
Select...
I am a veteran, but my wound severity score is less than 4.
Select...
I am a veteran without a severe infection.
Select...
I am not a veteran unable to walk.
Select...
My score is above 7.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ at each clinic visit through study completion, an average of 8 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~at each clinic visit through study completion, an average of 8 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Foot ulcer healing status
Foot ulcer size
Number of foot ulcers
+1 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Treatment groupExperimental Treatment2 Interventions
Patients will be given additional counseling
Group II: Control groupActive Control1 Intervention
Patients will be given standard of care.
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Who is running the clinical trial?
VA Office of Research and DevelopmentLead Sponsor
1,658 Previous Clinical Trials
3,361,463 Total Patients Enrolled
6 Trials studying Foot Ulcer
1,027 Patients Enrolled for Foot Ulcer
Muturi G. Muriuki, PhDPrincipal InvestigatorEdward Hines Jr. VA Hospital, Hines, IL
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I am a veteran with a detectable pulse in my feet.I am a veteran, but my wound severity score is less than 4.I am a veteran without a severe infection.I am not a veteran unable to walk.Veterans who are using a special walking boot for their diabetic foot ulcer can join the study.My score is above 7.If you score between 12 and 8, you may need extra help to understand the instructions.
Research Study Groups:
This trial has the following groups:- Group 1: Treatment group
- Group 2: Control group
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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