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Clinical Trial Summary

This pilot study was designed to test the safety of Celaderm(TM) in treating venous leg ulcers and to give preliminary information about the efficacy of two different Celaderm(TM) dosing regimens.


Clinical Trial Description

Celaderm(TM) weekly for four weeks or biweekly for four treatments combined with Profore(R) compression vs. Profore(R) compression alone. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00399308
Study type Interventional
Source Takeda
Contact
Status Completed
Phase Phase 1/Phase 2
Start date January 31, 2007
Completion date April 30, 2008

See also
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