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Clinical Trial Summary

The primary objective of this clinical investigation is to evaluate the debriding effect of ChloraSolv® on chronic (more than 1 moth) lower leg ulcer.


Clinical Trial Description

Approximately 58 subjects from at least two sites in Sweden will be included. Subjects presented with lower leg ulcer, covered with devitalised tissue for 50% or more and being candidate for cleansing, debridement/desloughing will be enrolled. Weekly application of Investigational Product for 6 weeks. Follow-up for wound status evaluation after 12 weeks from baseline. Total time in investigation is 12 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03808181
Study type Interventional
Source RLS Global
Contact
Status Completed
Phase N/A
Start date January 31, 2019
Completion date June 30, 2020