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CompletedNCT07621835PREDICORUpdated Jun 2, 2026

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

An observational study in CMV Specific Immune Response, Kidney Transplant and Kidney Transplant Recipient, sponsored by Maimónides Biomedical Research Institute of Córdoba. Completed at 1 site in Spain. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-06-02.

Sponsored by Maimónides Biomedical Research Institute of Córdoba · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
236
Ages
18 Years and older
Sex
All
01

Study 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.

Read the 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).

02

Conditions studied

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

Keywords

  • CMV
  • Kidney Transplantation
  • QuantiFERON-CMV
  • Solid Organ Transplantation
03

In context

Lead sponsor

Maimónides Biomedical Research Institute of Córdoba is the lead sponsor of 78 studies on the registry; 20 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

We will conduct a retrospective, observational, multicenter cohort study of CMV-seropositive (R⁺) kidney transplant recipients who did not receive ATG induction, between 1 January, 2019 and 30 April, 2025.

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

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
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
236 participants (actual)
Patient registry
No

Groups and cohorts

  • Derivation cohort

    The first phase will identify clinical and immunological risk factors associated with a non-reactive or indeterminate QF-CMV test result performed before day 45 post-transplant.

  • Validation cohort

    In the second phase, the risk factors identified in the derivation cohort will be tested in an independent cohort to validate their predictive value for the early absence of CMV-specific cellular immunity.

06

What researchers measure

Primary outcomes

  1. Risk factors associated with a non-reactive or indeterminate QF-CMV

    Absence of CMV-specific cellular immune response assessed by early QuantiFERON-CMV testing

    Time frame: Between 15 and 45 days after kidney transplantation

07

Study locations

1 site
  • HOSPITAL Universitario REINA SOFIA
    Córdoba, 14004, Spain
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07621835
Lead sponsor
Maimónides Biomedical Research Institute of Córdoba
Responsible party
Sponsor
First posted
Jun 2, 2026
Start date
Jan 1, 2019
Primary completion
Apr 30, 2025
Completion
Apr 30, 2025
Last update
Jun 2, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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