Diabetic Foot Ulcer Clinical Trial
Official title:
A Randomized, Placebo-controlled, Double-blind Phase II Study to Evaluate the Efficacy of IZN-6D4 Gel for the Treatment of Diabetic Foot Ulcers
Verified date | December 2015 |
Source | Izun Pharma Ltd |
Contact | n/a |
Is FDA regulated | No |
Health authority | Israel: Ministry of Health |
Study type | Interventional |
The purpose of this study is to determine if topical application of a hydrogel that contains plant extracts will improve healing of diabetic foot ulcers when compared to treatment with a hydrogel alone.
Status | Completed |
Enrollment | 82 |
Est. completion date | August 2015 |
Est. primary completion date | July 2015 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Current diagnosis of diabetes mellitus type 1 or 2 - Foot ulcer Wagner grade 1 or 2 - Ulcer between 1 square cm and 8 square cm present for at least 60 days and not more than two years - HgbA1C less than 10% - Able to comply with all procedures Exclusion Criteria: - Wound area decrease of greater than 30% between screening and baseline visits - Gangrene on any part of the affected foot - Pregnancy or lactation |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Israel | Wolfson Medical Center | Holon |
Lead Sponsor | Collaborator |
---|---|
Izun Pharma Ltd |
Israel,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The percent reduction in wound area at week 4 compared to the baseline visit | Weekly measurements of wound area from study initiation and through week 4 | No | |
Secondary | The percent conversion of the wound bed to granulation tissue by week 4 compared to baseline | Weekly assessments from baseline through week 4 | No | |
Secondary | The percentage of lesions that demonstrate at least 40% reduction in area by the end of week 4 compared to baseline visit | Weekly assessments of wound area through week 4 | No | |
Secondary | The percentage of lesions that demonstrate at least 50% reduction in area by the end of week 4 compared to baseline visit | Weekly assessments of wound area from baseline through week 4 | No |
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