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Clinical Trial Summary

2.1. Study Objectives - Primary Objective(s) - Identify the incidence and risk of CDI within one year after kidney, liver, and/or pancreas transplant - Secondary Objective(s) - Identify the risk factors for recurrent CDI post-transplant in patients who were diagnosed with a CDI within one year prior to Solid Organ Transplant - Evaluate the impact of CDI on graft survival following Solid Organ Transplant


Clinical Trial Description

- Single center, retrospective cohort chart review study design - Data will be collected on all liver, kidney, pancreas and combined transplant recipients who received their graft(s) from April 1, 2015 to July 31, 2018 - Will analyze outcomes from April 1, 2014 to July 31, 2019 - Patient list will be generated in Epic and Meditech - All data will be obtained from Epic and Meditech - All data will be collected retrospectively after the patient is discharged from the hospital ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04637321
Study type Observational
Source Methodist Health System
Contact
Status Completed
Phase
Start date November 4, 2019
Completion date August 7, 2020

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