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Risk Factors Associated With the Absence of CMV-specific Cellular Immune Response in the Early Post-transplant Period in Low-risk CMV-seropositive Kidney Transplant Recipients

Risk Factors Associated With the Absence of CMV-specific Cellular Immune Response in the Early Post-transplant Period in Low-risk CMV-seropositive Kidney Transplant Recipients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07621835
Acronym
PREDICOR
Enrollment
236
Registered
2026-06-02
Start date
2019-01-01
Completion date
2025-04-30
Last updated
2026-06-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

CMV Reactivation, CMV Specific Immune Response, Kidney Transplant, Kidney Transplant Recipient

Keywords

CMV, Kidney Transplantation, QuantiFERON-CMV, Solid Organ Transplantation

Brief summary

The goal of this observational study is to identify risk factors associated with the absence of CMV-specific cellular immune response in low-risk CMV-seropositive kidney transplant recipients in the early post-transplant period. The participant population includes adult CMV-seropositive kidney transplant recipients who did not receive antithymocyte globulin (ATG) induction therapy and underwent QuantiFERON-CMV testing within the first 45 days after transplantation. The main question it aims to answer is: \- Is it possible to predict which patients will fail to develop a CMV-specific cellular immune response before day 45 post-transplant in the absence of directly available immune assessment techniques? Researchers will compare patients with reactive QuantiFERON-CMV results to patients with non-reactive or indeterminate results to identify factors associated with the absence of CMV-specific cellular immune response. Participants will have retrospective clinical and laboratory data collected from medical records.

Detailed description

Study Hypothesis: In the absence of available techniques to assess CMV-specific cellular immunity, it may be possible to predict which patients will fail to develop a CMV-specific cellular immune response before day 45 post-transplant. Objective: Primary objective: * Derivation Cohort: To evaluate the risk factors associated with a non-reactive or indeterminate QF-CMV result before day 45 post-transplant in CMV-seropositive (R⁺) recipients who did not receive ATG prophylaxis. * Validation Cohort: To validate these risk factors in an independent validation cohort. Secondary Objectives: * To confirm whether patients with a non-reactive or indeterminate QF-CMV result before day 45 post-transplant and without ATG induction develop a higher rate of clinically significant CMV infection compared with those with a reactive QF-CMV result during the first 6 months post-transplant. * To confirm whether these same patients present a higher rate of viral replication during the first 6 months post-transplant. Study Population: The study will include adult patients (\>18 years) who are CMV-seropositive (R⁺), received a kidney transplant during the study period, did not receive ATG prophylaxis, and underwent QF-CMV testing on day 45 post-transplant (with a window period between day 30 and day 60 post-transplant).

Interventions

None listed

Sponsors

Maimónides Biomedical Research Institute of Córdoba
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Age \>18 years * Kidney or pancreas-kidney transplant recipients with positive CMV serology * QF-CMV test performed on day 45 post-transplant (window period between day 30 and day 60 post-transplant) * CMV PCR testing performed at least every two weeks during the first three months post-transplant

Exclusion criteria

* HIV-infected patients * Multivisceral transplant recipients * Patients scheduled to receive universal prophylaxis despite having a reactive QF-CMV result * Patients who received ATG induction therapy * Less than 6 months of post-transplant follow-up

Design outcomes

Primary

MeasureTime frameDescription
Risk factors associated with a non-reactive or indeterminate QF-CMVBetween 15 and 45 days after kidney transplantationAbsence of CMV-specific cellular immune response assessed by early QuantiFERON-CMV testing

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 3, 2026