Study to Evaluate the Efficacy and Tolerability of Venaflon Use in Reducing the Symptoms Caused by Chronic Venous Insufficiency When Compared With Daflon
This study is not yet open for participant recruitment.
Verified November 2011 by Laboratório Teuto Brasileiro S/A
Sponsor:
Laboratório Teuto Brasileiro S/A
Information provided by (Responsible Party):
Laboratório Teuto Brasileiro S/A
ClinicalTrials.gov Identifier:
NCT01477281
First received: October 19, 2011
Last updated: November 18, 2011
Last verified: November 2011
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No Study Results Posted on ClinicalTrials.gov for this Study
| Study Status: | This study is not yet open for participant recruitment. |
|---|---|
| Estimated Study Completion Date: | August 2012 |
| Estimated Primary Completion Date: | July 2012 (Final data collection date for primary outcome measure) |