Clinical Evaluation of the QuantiFERON CMV Assay

NCT03502161 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 8

Last updated 2020-09-16

No results posted yet for this study

Summary

Validate the use of the device in the clinical setting for assessing the risk of CMV Infection in SOT recipients after the completion of antiviral prophylaxis.

Conditions

  • CMV

Interventions

DEVICE

QuantiFERON CMV Assay

Assay to measure cell-mediated immune function using QuantiFERON CMV assay.

Sponsors & Collaborators

  • QIAGEN Gaithersburg, Inc

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-11-15
Primary Completion
2020-05-15
Completion
2020-06-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03502161 on ClinicalTrials.gov