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Clinical Trial Summary

The study will prospectively determine the clinical utility of CMV cell-mediated immunity using the Quantiferon test. The investigators will use the assay results to tailor the duration of CMV prophylaxis in solid organ transplant patients.


Clinical Trial Description

Cytomegalovirus (CMV) disease is an important cause of morbidity in solid organ transplantation recipients and remains the most common opportunistic viral infection in these patients. Standard CMV prevention strategies include universal prophylaxis and pre-emptive therapy with viral load monitoring. However, neither of these strategies has been successful in eliminating CMV disease as seen by high rates of viremia, incidence, and CMV recurrence despite treatment. Recently, the Quantiferon-CMV assay has been shown to predict late CMV reactivation after prophylaxis and to be predictive of viral progression and the need for antiviral therapy in organ transplant recipients who develop low level CMV viremia. The purpose of the current study is to test the clinical strategy of using the Quantiferon-CMV assay in guiding the duration of primary CMV prophylaxis in solid organ transplant patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02784756
Study type Interventional
Source University Health Network, Toronto
Contact
Status Completed
Phase N/A
Start date June 2016
Completion date April 2020

See also
  Status Clinical Trial Phase
Completed NCT02370758 - Cell Mediated Immunity for Secondary Prophylaxis in CMV SOT Patients N/A
Unknown status NCT01397058 - Reactivation of CMV Infection in Immunocompetent Patients Under Severe Stress N/A