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Clinical Trial Summary

This study will test the safety and efficacy of nitric oxide gas in the treatment of venous leg ulcers


Clinical Trial Description

Prospective, single center. Controlled study of a moisture retentive wound dressing and sustained compression with 6 weeks of 8 hour daily nitric oxide treatments. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00545298
Study type Interventional
Source Nitric BioTherapeutics, Inc
Contact
Status Terminated
Phase Phase 2
Start date October 2007
Completion date November 2008

See also
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