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RecruitingNCT05661032ResVirUpdated Sep 17, 2026

Novel Technologies for Respiratory Virus Identification

An observational study in Infections, Respiratory and Respiratory Tract Infections, sponsored by Portsmouth Hospitals NHS Trust. Recruiting at 1 site in United Kingdom. Per ClinicalTrials.gov, last updated 2026-09-17.

Sponsored by Portsmouth Hospitals NHS Trust · Observational

From the registry’s dates

  • Started Jan 2023; still recruiting 3 years 9 months later.
Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
1,000
Sex
All
01

Study summary

Current virus detection methods often take significant time or can be limited in sensitivity, specificity or cost. There is therefore a need for diagnostic methods that are simple to use, sensitive, rapid and inexpensive.

This is a proof of concept study to determine whether the Pictura Bio system (a new a rapid pathogen identification technology) is able to detect and differentiate different viruses from nasopharyngeal swabs/aspirate specimens. The data collected will be used to "train" the algorithms to be able to accurately identify respiratory viruses. The accuracy with which the algorithms estimate the test dataset will be monitored at regular intervals during the training dataset collection period. The Pictura Bio system is still under development, which means that it is still "learning". The system needs to see more information so that it can be sufficiently accurate to be used in clinical practice and should become more accurate in identifying these viruses as it sees more and more information from patients.

This study will take place at Portsmouth Hospitals University NHS Trust and aims to recruit 1000 patients. To do this, we will recruit both adults and children who either present to the emergency department or are admitted to QAH with a clinical suspicion of a respiratory viral infection. All participants will have a nose and/or throat swab taken as part of their clinical assessment, and we would ask to take a further nasal swab for the purpose of the study. Research sampling will be combined with routine clinical samples where possible to reduce the frequency of testing. We will use most of the information to teach the system how to become more accurate at identifying respiratory viruses. We will keep the remaining information separate and use it to test how accurate the system is. All of the data will be kept securely. Basic information will be collected including age, gender, results of blood tests taken for clinical review, treatment and outcome data. No results from the swabs taken for the purpose of the study will be available to either the participant or the clinical team and the information will have no effect on patient care.

Read the detailed description

NHS services always come under pressure over the winter period as demand for hospital services increase with the arrival of cold weather and the increase spread of respiratory infections.

As hospitals now look beyond the COVID-19 pandemic, the need to meet future hospital service challenges are important. Changes in habit and measures put in place to control the spread of COVID-19 have affected the transmission of other respiratory viruses. Understanding changes in occurrences of respiratory like illnesses during the winter period could help in understanding future winter pressures for healthcare services.

Since viral and bacterial infection symptoms can be similar, broad spectrum antibiotics are often used as the first line of defence even when the cause of infection is unknown. Antibiotics are not effective against viral infections and only work against bacteria. Antibiotics prevent millions of deaths each year however, inappropriate prescription rates and overuse have led to antibiotic resistance that has created a global health emergency in superbugs resistant to these treatments. There is a need for rapid and sensitive tests to diagnose the cause of infection and ensure patients get the most suitable type of treatment.

THE TECHNOLOGY The hospital is working closely with Pictura Bio, who are developing a rapid pathogen identification technology comprising microscope and a computer which is trained to recognise fluorescent patterns from different viruses. The performance of this AI algorithm is highly dependent on the quality of the samples used to train it. It has the potential to be quicker than current gold standard technology and could be used in a patient facing setting including GP surgeries and Pharmacies.

THE RESEARCH STUDY This is a proof of concept study to determine whether the Pictura Bio system is able to detect and differentiate different viruses from nasopharyngeal swabs/aspirate specimens. The data collected will be used to "train" the algorithms to be able to accurately identify respiratory viruses. The accuracy with which the algorithms estimate the test dataset will be monitored at regular intervals during the training dataset collection period. The Pictura Bio system is still under development, which means that it is still "learning". The system needs to see more information so that it can be sufficiently accurate to be used in clinical practice and should become more accurate in identifying these viruses as it sees more and more information from patients.

This study will take place at Portsmouth Hospitals University NHS Trust and aims to recruit 1000 patients. To do this, we will recruit both adults and children who either present to the emergency department or are admitted to QAH with a clinical suspicion of a respiratory viral infection. All participants will have a nose and/or throat swab taken as part of their clinical assessment, and we would ask to take a further nasal swab for the purpose of the study. Research sampling will be combined with routine clinical samples where possible to reduce the frequency of testing. We will use most of the information to teach the system how to become more accurate at identifying respiratory viruses. We will keep the remaining information separate and use it to test how accurate the system is. All of the data will be kept securely. Basic information will be collected including age, gender, results of blood tests taken for clinical review, treatment and outcome data. No results from the swabs taken for the purpose of the study will be available to either the participant or the clinical team and the information will have no effect on patient care.

SHARING OF FINDINGS Results of the study will be disseminated via paper submissions to relevant journals and conferences. A lay summary of the results will be produced in collaboration with the PHT PRA group. The study team will explore with this group other avenues and formats for the dissemination of the study findings to ensure as wide a public audience as possible, for example through co-produced public talks, articles in community communications and social media.

02

Conditions studied

  • Infections, Respiratory
  • Respiratory Tract Infections
03

In context

Respiratory Tract Infections

751 studies on the registry are indexed under Respiratory Tract Infections; 114 are open to participants now.

This study's planned enrollment of 1,000 is above the median of 350 across 184 observational studies indexed under Respiratory Tract Infections.

Browse Respiratory Tract Infections studies →

Lead sponsor

Portsmouth Hospitals NHS Trust is the lead sponsor of 74 studies on the registry; 14 are open to participants now.

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

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Sampling method
Probability sample

Study population

Anybody with a suspected or confirmed respiratory virus illness (including both staff and patients)

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Provide informed, (parental/guardian, where appropriate) consent
  • Able to provide nasopharyngeal swab/aspirate specimens.
  • A clinical suspicion of a respiratory viral infection with one or more of the following symptoms:
  • Coryzal symptoms (runny nose, sneezing and/or nasal congestion)
  • New onset of cough
  • Sore throat
  • Head and/or Muscle aches
  • Fever or chills

Exclusion criteria

Exclusion Criteria:

  • Unable to comply with study procedures or where in the opinion of the investigator, undertaking a nasopharyngeal swab may be detrimental to the individual
  • Lacking capacity to consent
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
1,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • Covid Positive

    Nasopharyngeal Swab

  • Covid Negative

    Nasopharyngeal Swab

06

What researchers measure

Primary outcomes

  1. The Pictura Bio system to detect viral pathogens from human derived samples

    To determine whether the Pictura Bio system is able to detect viral pathogens from human derived samples compared with gold standard methodologies used in NHS diagnostic settings

    Time frame: Until 01/03/2026

  2. Create a fluorescent based viral data pattern database

    To create a fluorescent based viral data pattern database from human samples which can be used to interrogate machine learning algorithms to improve sensitivity and specificity for continued development of the technology

    Time frame: Until 01/03/2026

Secondary outcomes

  1. The prevalence of seasonal respiratory viruses in the local hospital community

    Observe the prevalence of seasonal respiratory viruses in the local hospital community following the lifting of previous COVID restrictions to help direct future local IPC guidelines

    Time frame: Until 01/03/2026

  2. Prevalence use of antibiotics for respiratory infections

    Observe the use of antibiotics for respiratory infections to help understand prescribing patterns and any over or under use

    Time frame: Until 01/03/2026

07

Study locations

1 of 1 sites recruiting
  • Portsmouth Hospitals NHS Trust, Queen Alexandra Hospital
    Portsmouth, Hampshire PO6 3LY, United Kingdom
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 17, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05661032
Lead sponsor
Portsmouth Hospitals NHS Trust
Responsible party
Sponsor
First posted
Dec 22, 2022
Start date
Jan 18, 2023
Primary completion
Jun 30, 2027 (estimated)
Completion
Jun 30, 2027 (estimated)
Last update
Sep 17, 2026

Study contacts

Yvette Hibberd
Contact
Yvette.hibberd@porthosp.nhs.uk
023 9228 6000 ext. 5153
Joe Shoebridge
Contact
joe.shoebridge@porthosp.nhs.uk
023 9228 6000 ext. 5153
Sharon Glaysher, Dr
principal investigator · Portsmouth University Hospital NHS Trust

Oversight

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

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