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NCT Number: NCT07787767

CMV Refractory and Resistant Infection in Solid Organ Transplant Recipients in Argentina

This study will describe the frequency and characteristics of refractory and resistant cytomegalovirus (CMV) infection in adults who received a solid organ transplant in Argentina between 2017 and 2024. Researchers will review medical records from transplant centers across the country to identify episodes of CMV infection that did not respond adequately to standard antiviral treatment (refractory) or that showed genetic mutations associated with drug resistance. The study will describe the clinical features, treatments used, and outcomes (including graft function and survival) of patients with these episodes, in order to better understand how common this problem is and what factors are associated with it in the local population.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Hospital Italiano de Buenos Aires

Buenos Aires, Buenos Aires F.D., 1199, Argentina

Location contact

Astrid Smud, MD

SUB_INVESTIGATOR

EMILIO Felipe HUAIER ARRIAZU, MD

CONTACT

[email protected]

+54911-49590200 ext. 8165 / 9542

Emilio Felipe Huaier Arriazu, MD

SUB_INVESTIGATOR

Laura Alicia Barcan, MD

CONTACT

[email protected]

+54911-49590200 ext. 8206

Laura Alicia Barcan, MD

PRINCIPAL_INVESTIGATOR

Natalia Pujato, MD

SUB_INVESTIGATOR

About this study

Cytomegalovirus (CMV) remains one of the most frequent infections after solid organ transplantation (SOT), with important direct and indirect effects on graft and patient survival. While preventive strategies (prophylaxis and preemptive therapy) have reduced CMV-related disease and mortality, refractory and resistant CMV infection continues to be a major challenge, particularly in high-risk transplants (donor-positive/recipient-negative serostatus, and those receiving thymoglobulin induction). No epidemiological data on refractory or resistant CMV currently exist in Argentina.

This multicenter retrospective cohort study will include adult (≥18 years) solid organ transplant recipients from participating centers in Argentina who developed CMV infection within 18 months post-transplant, between January 1, 2017 and December 31, 2024. Cases meeting pre-specified operational criteria for refractory or resistant CMV infection will be identified from medical records. Refractory infection is defined as viral load that does not decrease or increases after two weeks of appropriate antiviral treatment; resistant infection is defined as refractory infection with documentation of at least one genetic mutation (UL97 and/or UL54) associated with antiviral resistance, confirmed through genotyping performed at the national reference laboratory (Instituto Malbrán).

Data will include demographic and transplant-related variables, immunosuppression regimen, virological monitoring, antiviral treatment lines and dosing, resistance genotyping results when available, and clinical outcomes including graft function, rejection episodes, and mortality at 90 days and one year. Data will be collected, coded, and stored in a centralized, de-identified database (REDCap) for descriptive and comparative statistical analysis.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patients (≥18 years) who received a solid organ transplant (kidney, liver, heart, lung, pancreas, or combined) at a participating center in Argentina between January 1, 2017 and December 31, 2024
  • Documented CMV infection within 18 months post-transplant
  • Followed for at least 18 months from transplant and at least 12 months from CMV infection onset

Exclusion criteria

  • Patients with incomplete medical records precluding assessment of CMV infection status or key study variables
  • Patients not meeting the minimum follow-up period from transplant or from infection onset

Treatment and study plan

Primary outcomes

  1. Incidence of refractory or resistant CMV infection

    Time frame: Within 18 months post-transplant, assessed retrospectively for the period January 2017 to December 2024

    Proportion of solid organ transplant recipients with CMV infection who meet operational criteria for refractory infection (viral load unchanged or increased after 2 weeks of appropriate antiviral treatment) or resistant infection (refractory infection plus documented genetic mutation, e.g. UL97 and/or UL54, associated with antiviral resistance)

Secondary outcomes

  1. Incidence of overall CMV infection

    Time frame: Within 18 months post-transplant, 2017-2024

    Proportion of SOT recipients with any CMV infection (primary infection, reactivation, asymptomatic infection, or disease), stratified by transplanted organ

  2. Distribution of clinical forms of CMV infection

    Time frame: Within 18 months post-transplant, 2017-2024

    Classification of CMV episodes as primary infection, reactivation, asymptomatic infection, or CMV disease

  3. Frequency of antiviral resistance mutations

    Time frame: From T3 (declaration of refractoriness) to T4 (episode resolution), up to 12 months

    Proportion of genotyped refractory CMV episodes with ≥1 resistance-associated mutation (UL97 and/or UL54)

  4. Antiviral treatment lines and combination therapy use

    Time frame: From T2 (treatment initiation) to T4 (negativization) or last available PCR if not resolved, up to 12 months

    Number of antiviral treatment lines used per episode (1, 2, ≥3) and proportion of episodes receiving combination antiviral therapy (≥2 active agents ≥72h)

  5. All-cause mortality

    Time frame: 90 days and 1 year post-episode onset

    Proportion of patients who died at 90 days and at 1 year after the CMV refractory/resistant episode

  6. Graft outcome

    Time frame: rejection following the CMV refractory/resistant episode Through 1 year post-episode onset

    Proportion of patients with graft loss or rejection following the CMV refractory/resistant episode

  7. Association between mutation type and antiviral treatment received

    Time frame: From T2 (antiviral treatment initiation) to T4 (episode resolution), up to 12 months

    Distribution of antiviral treatment regimens received (ganciclovir, foscarnet, letermovir, maribavir, cidofovir, combination therapy) according to mutation type detected (UL97 vs. UL54 vs. none)

  8. Virologic response

    Time frame: From T2 (treatment initiation) to T4 (confirmed negativization), up to 12 months, with censoring at last available PCR for patients not achieving negativization

    Time to virologic negativization (two consecutive negative PCR results ≥7 days apart)

Study contacts

Contact information is provided by the study sponsor or research team.

Emilio Felipe Huaier Arriazu, MD

CONTACT

[email protected]

+549 011 49590200 ext. 8165 / 9542

Laura Alicia Barcan, MD

CONTACT

[email protected]

+549 1149590200 ext. 8206

Sponsors and collaborators

Lead sponsor

Hospital Italiano de Buenos Aires

Other

Collaborators

  • Takeda Pharmaceuticals North America, Inc.

Registry information

Official study title

Evaluation of Cytomegalovirus Refractoriness and Resistance in Solid Organ Transplantation in Argentina: A Multicenter Study

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Aug 26, 2026
Registry last updated
Aug 26, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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