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Clinical Trial Summary

This study is to compare the efficacy and safety of Medifoam® and Betafoam®, which is a new dressing that contains povidone-iodine, in patients with diabetes foot ulcer. 70 patients (35 each arm) are targeted to be enrolled in this study. Treatment follow periods are 8weeks.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02732886
Study type Interventional
Source Mundipharma Korea Ltd
Contact
Status Completed
Phase N/A
Start date March 29, 2016
Completion date September 29, 2017

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