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Clinical Trial Summary

The study is a prospective, single arm, post- marketing study. The subjects enrolled to the study will receive weekly applications of ActiGraft until complete healing or until investigator's decision that patient can no longer benefit from the study treatment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04745806
Study type Interventional
Source RedDress Ltd.
Contact Sahar Boostenay
Phone +972544621243
Email sboostenay@reddressmedical.com
Status Recruiting
Phase N/A
Start date March 1, 2021
Completion date April 1, 2022

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