CClinicalTrials.gg
CompletedNCT02324244Updated Dec 24, 2014

CMV Intensive Care Units

An observational study in CMV Infection, sponsored by Emilio Bouza. Completed at 1 site in Spain. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2014-12-24.

Sponsored by Emilio Bouza · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
150
Ages
18 Years and older
Sex
All
01

Study summary

Prospectively assessment of CMV viremia by real-time polymerase chain reaction (PCR) in a broad cohort of consecutive immunocompetent adults admitted to a major heart surgery intensive care unit (MHS-ICU) with the goal of determining the epidemiology, risk factors, and clinical significance of CMV infection.

02

Conditions studied

  • CMV Infection

Keywords

  • Cytomegalovirus
  • critical patient
  • ICU
  • immunocompetent
  • clinical suspicion
  • risk factors
03

In context

Infections

6,686 studies on the registry are indexed under Infections; 807 are open to participants now.

This study's enrollment of 150 is below the median of 240 across 2,136 observational studies indexed under Infections.

Browse Infections studies →

Lead sponsor

Emilio Bouza is the lead sponsor of 5 studies on the registry; none 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
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

immunocompetent adults admitted to a major heart surgery intensive care unit

Inclusion criteria

  • Agreeing to participate in the study
  • Age of at least 18 years
  • Admission to the MHS-ICU for at least 72 hours

Exclusion criteria

Exclusion Criteria:

  • Inability to give informed consent
  • Age younger than 18 years
  • AIDS
  • Pregnancy
  • Organ or bone marrow transplant, receipt of immunosuppressive therapy including corticosteroids within 30 days, and cancer or hematologic malignancy treated with radiotherapy or chemotherapy
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
150 participants (actual)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • immunocompetent patients underwent heart surgery
06

What researchers measure

Primary outcomes

  1. incidence number of participants with a positive CMV positive result

    Time frame: month 8

Secondary outcomes

  1. risk factors for CMV reactivation

    Time frame: month 8

  2. mortality by day 30

    composite endpoint. hospitalization or death by day 30

    Time frame: month 8

  3. prolonged hospitalization . More than 30 days

    Time frame: month 8

07

Study locations

1 site
  • Servicio de Microbiologia y Enfermedades Infecciosas
    Madrid, 28007, Spain
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 24, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02324244
Lead sponsor
Emilio Bouza
Responsible party
Emilio Bouza (Head of Department, Hospital General Universitario Gregorio Marañon) — Sponsor-investigator
First posted
Dec 24, 2014
Start date
Oct 2012
Primary completion
May 2013
Completion
May 2013
Last update
Dec 24, 2014

Study contacts

Patricia Muñoz, PhD
principal investigator · Hospital General Universitario Gregorio Marañon

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2014. You cannot join it, but the record below documents what was studied.

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