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Clinical Trial Summary

Johns Hopkins clinical research office quality assurance group will monitor and audit this study at Johns Hopkins. The Sub Investigator at each site will be responsible for internal monitoring at their site.


Clinical Trial Description

The Sub Investigator at each site will be responsible for internal monitoring at their site. The site sub Investigator and study team will report any serious adverse events to Principal Investigator and annually report adverse events. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02000089
Study type Interventional
Source Johns Hopkins University
Contact Hilary Cosby, RN
Email hcosby1@jhmi.edu
Status Recruiting
Phase Phase 3
Start date January 6, 2014
Completion date December 2025

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