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Not Yet Recruiting NCT05708755

CMV Immunity Monitoring in Lung Transplant Recipients

Conditions: Lung Transplant; Complications

Sex: All
Ages: 18 Years – 99 Years
Phase: PHASE2
Enrollment: 50
Sponsor: NYU Langone Health

Location: United States

Summary

The purpose of this study is to determine the safety and feasibility of using a laboratory test to guide duration of antiviral prophylaxis with valganciclovir (medication used to prevent viral infections) after lung transplant. The laboratory test, inSIGHT™ CMV T Cell Immunity Panel, measures patients' immune response to a common viral infection known as cytomegalovirus (CMV). The goal of this study will be to safely decrease how long patients need to take valganciclovir based on the results of the CMV T Cell Immunity Panel.

Eligibility Criteria

Inclusion Criteria:Received a lung transplant, or multi-organ transplant involving a lung at NYU Langone HealthPre-existing serological immunity to CMV (R+)Able and willing to provide informed consentExclusion Criteria:Anti-thymocyte globulin induction immunosuppressionPerioperative desensitizationPregnant or breastfeeding women

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05708755). StuddyBuddy aggregates publicly available trial information.