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Anti-infective Irrigation Therapy
vancomycin-tobramycin-itraconazole for Foot Ulcer
Phase < 1
Waitlist Available
Led By Laura R Vick, MD
Research Sponsored by University of Mississippi Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 weeks
Awards & highlights
All Individual Drugs Already Approved
Approved for 10 Other Conditions
No Placebo-Only Group
Summary
This trial is testing a special liquid treatment to help heal foot sores in people with diabetes. The treatment is used regularly to clean and fight infections in the sores. The goal is to see if this treatment can help more sores heal and reduce the need for amputations.
Eligible Conditions
- Foot Ulcer
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Healing Rate
Secondary study objectives
Wound Closure
Awards & Highlights
All Individual Drugs Already Approved
Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
Approved for 10 Other Conditions
This treatment demonstrated efficacy for 10 other conditions.
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Treatment of Diabetic Foot UlcerExperimental Treatment1 Intervention
Participants with diabetic foot ulcers will be treated with a compounded, anti-infective irrigation therapy daily until closure of the ulcer or up to a maximum of 3 months. This is an irrigating foot bath with a compounded medication of vancomycin-tobramycin-itraconazole. This medication with combined 3/4 gallon of water. Participant will soak foot in solution for 10 minutes per day. Daily until wound is healed for a minimum of 4 weeks and a maximum of 3 months.
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Who is running the clinical trial?
University of Mississippi Medical CenterLead Sponsor
179 Previous Clinical Trials
196,621 Total Patients Enrolled
Keystone PharmacyUNKNOWN
Laura R Vick, MDPrincipal InvestigatorUniversity of Mississippi Medical Center
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