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Clinical Trial Summary

The investigation is designed as an open, randomized, non-inferiority, multi-centre investigation. 212 evaluable subjects will be randomised. Subjects to be included will suffer from an exuding venous or mixed ulcer of predominantly venous origin. Subjects will either be randomized to Exufiber®Gelling Fibre Dressing or Aquacel®Extra Hydrofiber® Dressing with Strengthening Fibre using, centralized randomization


Clinical Trial Description

Visits are planned for baseline followed by 1, 2, 3, 4 and 6 weeks post treatment. The sub-group of at least 50 subjects will also be followed at week 8, 12, 16, 20, and 24 post treatment or until wound is healed if earlier. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02921750
Study type Interventional
Source Molnlycke Health Care AB
Contact
Status Completed
Phase N/A
Start date October 2016
Completion date November 27, 2019

See also
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