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CompletedNCT02538770Updated Jan 11, 2016

Rapid Viral Diagnostics in Adults to Reduce Antimicrobial Consumption and Duration of Hospitalization

An interventional study of Rapid diagnostics using Anyplex TMII RV16 Detection and Delayed diagnostics Anyplex TMII RV16 Detection in Respiratory Virus Infection, Fever of Unknown Origin and Dyspnea, sponsored by University of Oulu. Completed at 2 sites in Finland. Open to participants aged 16 Years and older. Per ClinicalTrials.gov, last updated 2016-01-11.

Sponsored by University of Oulu · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
900
Allocation
Randomized
Ages
16 Years and older
Sex
All
01

Study summary

Viral respiratory infections are common and often require use of health care resources. Patients receive inappropriate bacterial antibiotics, which has many problems including side-effects, development of resistance and costs.

A small portion of the infections leads to severe clinical manifestations including hospitalisations and deaths. The significance of influenza virus is well known and it is actively detected in all age groups. However, the benefits of detecting other respiratory viruses have mainly been studied among children but not among adults. The development of multiplex PCR technique has provided a new and sensitive method for diagnosing a large panel of viruses. To convince the economical benefits of the rapid viral diagnostic in adult infectious patient, more evidence is needed.

In our randomized study, nasal and pharyngeal samples from the patients evaluated at the emergency clinic of internal medicine in the University Hospital of Oulu because of any respiratory symptom, chest pain or fever, will be collected. The samples will be tested for 16 different respiratory viruses by using Anyplex TMII RV16 Detection. The adult participants will be randomized in two groups. In one group the results of the testing will be reported for the attending physician as soon as possible, and in the other group 7 days after sampling. The effect of this delay to patient care is monitored. Also the results of children and adults are compared as well as results of men and women. The hypothesis is that rapid viral diagnostics shortens the length of admission and diminishes the use of bacterial antibiotics. New information on the viral epidemiology among children and adults is provided and clinical manifestations of specific viral infections in adults are described.

The estimated 1500 samples are also tested for 5 different respiratory bacteria by Anyplex TM II RB5 Detection. These results will be examined after completion of the study period. The benefits of rapid bacterial detection are evaluated in respect to the clinical course of the disease and considering the infection control aspects as well.

Read the detailed description

Aim and Hypothesis

The aim of the study is:

  1. To find out how the modern rapid multiplex-PCR based respiratory virus detection method affects the patient care
  2. To examine does it shorten the length of admission and reduce antibiotic consumption
  3. Compare the seasonality of different viruses in children and adults
  4. Investigate the development and progress of an epidemic
  5. Study the differences in the prevalence and severity of infections between genders
  6. Describe clinical manifestations of different viral infections in adults
  7. View more closely certain subgroups such as patients with chest pain in respect to different viral epidemics and their effect on the hospital admission rates
  8. Evaluate the information provided by the bacterial detection

Subjects Our hospital is both a regional and a university hospital at the same time. Patients come to our clinic from a quite large area surrounding the city of Oulu and they represent the general population of the area well. The study population will be recruited 2014-2015 in the emergency clinics for pediatric and internal medicine patients in the Oulu University Hospital. Participants are patients with respiratory infection symptoms, chest pain or fever. Fever is determined as body temperature of 38 degrees centigrade or more measured either in the hospital or at home.

Study design This is a randomized clinical trial evaluating the impact of modern multiplex PCR based respiratory virus diagnostics on treatment and outcome of adult patients. Participants are randomized in two groups with results being reported either immediately or after a week (Picture 1). In children the viral PCR diagnostics is already routinely used and collection of nasal and pharyngeal samples continues normally. All pediatric results are reported immediately. Approval of the ethical review board of the Northern Ostrobothnia Hospital District has been acquired.

Course of the study Data collection All patients entering the internal medicine emergency clinics because of respiratory infection symptoms (cough, rhinitis, shortness of breath, sore throat), chest pain or fever will be given the opportunity to participate in the study. After signing an informed consent a nasal and a pharyngeal swab will be taken for viral examination. Adult patients are randomized in two different groups. In one group the results of the viral detection are reported immediately and in the other group they are reported 7 days after sampling.

Samples will be analyzed in the microbiological laboratory by real time PCR method Anyplex TMII to detect genome of 16 different respiratory viruses and of 5 different bacterial pathogen (Table 1). Results in the delayed group will be given earlier in the case the clinician is requesting them. The results of the bacterial findings will be analyzed after completion of the study since the clinical relevance of them is not clear yet. The bacteriological diagnostic of the patients during the study relies on the routinely used methods.

The attending clinician decides the treatment and care of the patient independently. Patient's chart will be reviewed for the course of disease, antibiotic use, ICU care and length of hospital stay. The results of key laboratory tests and microbiological findings will be collected. Radiological findings will be registered. At discharge, the participants are asked to report the duration of the symptoms, absence from work and the date of a possible doctors follow up. The population register centre will be used at the end of the study to find out the number of deceased, and their time and cause of the death will be recorded

. Table 1. Microbes detected from the study samples Viruses (AnyplexTMII RV16 Detection) Adenovirus Influenza A/B virus Parainfluenza virus1/2/3/4 Rhinovirus A/B/C Respiratory syncytial virus A/B Bocavirus 1/2/3/4 Metapneumovirus Coronavirus 229E/NL63/OC43 Enterovirus

Data analysis The length of hospital admission and the use of bacterial antibiotics is compared between the randomized groups. Viral findings of children and adults will be evaluated. The emergence of viruses in different areas of the district as well as in different age groups is examined. The differences in clinical picture and in microbiological findings between genders are viewed. The symptoms and clinical findings in adults with detected RSV or metapneumovirus are described. The bacterial findings are evaluated and compared with clinical data to determine the significance of the information provided by the test.

Impact of the study In our hospital major part of the viral respiratory infection diagnostics in adults has been accomplished by influenza virus antigen detection. Now a more sensitive measure for detecting 16 different respiratory pathogens from nasopharyngeal sample is available. We will determine whether more specific identification of the etiological agent affects the patient care. If the accurate diagnostics diminishes inappropriate antibiotic use it saves the patient from potential side effects and the society from unnecessary costs. Importantly it also saves the microbial flora from the antibiotic selection pressure which is considered to facilitate the emergence of antibiotic resistance. In children the benefits of accurate diagnostics have been recognized but in adults this is still under progress. This study is designed to demonstrate these advantages in adults.

02

Conditions studied

  • Respiratory Virus Infection
  • Fever of Unknown Origin
  • Dyspnea
  • Chest Pain

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03

In context

Dyspnea

656 studies on the registry are indexed under Dyspnea; 153 are open to participants now.

This study's enrollment of 900 is above the median of 48 across 430 interventional studies indexed under Dyspnea.

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Lead sponsor

University of Oulu is the lead sponsor of 138 studies on the registry; 21 are open to participants now.

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

04

Who can participate

Ages eligible
16 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • All patients visiting Oulu University Hospital emergency room or admitted to acute pulmonology ward AND signs of possible respiratory tract infection such as cough, fever or dyspnea OR chest pain

Exclusion criteria

Exclusion Criteria:

  • No exclusion criteria
05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
900 participants (actual)

Study arms

  • Experimental
    Rapid Anyplex TMII RV16 Detection

    Intervention is the rapid performance of Anyplex TMII RV16 detection

    Other: Rapid diagnostics using Anyplex TMII RV16 Detection

  • Active comparator
    Delayed Anyplex TMII RV16 Detection

    Comprative intervention is the delayed performance of Anyplex TMII RV16 detection

    Other: Delayed diagnostics Anyplex TMII RV16 Detection

Interventions

  • OtherRapid diagnostics using Anyplex TMII RV16 Detection

    Rapid diagnostics using Anyplex TMII RV16 Detection, i.e. physician receives results of respiratory virus PCR as soon as they are available

  • OtherDelayed diagnostics Anyplex TMII RV16 Detection

    Delayed diagnostics Anyplex TMII RV16 Detection, i.e. physician receives results of respiratory virus PCR after one week delay unless specifically solicited

06

What researchers measure

Primary outcomes

  1. Duration of hospitalization

    The number of days in hospital within one month after randomization

    Time frame: One month

  2. Antimicrobial consumption

    Number of days on antimicrobials within one month after randomization

    Time frame: One month

  3. Antimicrobial consumption

    Defined daily doses of antimicrobial agents within one month after randomization

    Time frame: One month

Secondary outcomes

  1. Number of radiological examinations

    Time frame: One month

  2. Cost of other examinations in hospital

    Time frame: One month

07

Study locations

2 sites
  • Emergency Room of Oulu University Hospital
    Oulu, Finland
  • Pulmonology ward Oulu University Hospital
    Oulu, Finland
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 11, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02538770
Lead sponsor
University of Oulu
Collaborators
Oulu University Hospital
Responsible party
Sponsor
First posted
Sep 2, 2015
Start date
Sep 2014
Primary completion
Nov 2015
Completion
Nov 2015
Last update
Jan 11, 2016

Study contacts

Marjo Renko, PhD, MD
principal investigator · Oulu University Hospital

Oversight

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

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This study is completed, as verified in Jan 2016. You cannot join it, but the record below documents what was studied.

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