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Clinical Trial Summary

The purpose of this study is to estimate the proportion of Ventricular Assist Device (VAD) patients with abnormal gastrointestinal bleeding as assessed by HemoQuant fecal occult blood test. Also, in patients with gastrointestinal bleeding present, to summarize the extent of gastrointestinal bleeding; to examine the behavior of HemoQuant fecal occult blood test over time by estimating the proportion of VAD patients with a positive test prior to implantation; at one week, one month, three months, six months and one year post implantation, and after explantation of the VAD and to evaluate whether presence of any abnormal fecal HemoQuant test is predictive of a future major bleeding event.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01415869
Study type Observational
Source Mayo Clinic
Contact
Status Completed
Phase
Start date June 22, 2011
Completion date June 22, 2013

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