Clinical Trials Directory

Trials / Completed

CompletedNCT01415869

Occult Gastrointestinal Bleeding in Non-pulsatile Left Ventricular Assist Device(VAD)Patients

Status
Completed
Phase
Study type
Observational
Enrollment
38 (actual)
Sponsor
Mayo Clinic · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Timeline

Start date
2011-06-22
Primary completion
2013-06-22
Completion
2013-06-22
First posted
2011-08-12
Last updated
2019-05-20

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01415869. Inclusion in this directory is not an endorsement.