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RASCALS: Rapid Assay for Sick Children With Acute Lung Infection Study

RASCALS: Rapid Assay for Sick Children With Acute Lung Infection Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04233268
Acronym
RASCALS
Enrollment
250
Registered
2020-01-18
Start date
2020-06-06
Completion date
2025-02-28
Last updated
2021-10-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID19, Lower Respiratory Tract Infection, Ventilator Associated Pneumonia

Brief summary

Lower Respiratory Tract infections are a common cause of admission to the intensive care unit. Children routinely receive antibiotics until the tests confirm whether the infection is bacterial or viral. The exclusion of bacterial infection may take 48 hours or longer for culture tests on biological samples to be completed. In many cases, the results may be inconclusive or negative if the patient has already received antibiotics prior to the sample being taken. A rapid assay to detect the most likely cause of infection could improve the speed with which antibiotic therapy is rationalised or curtailed. This study aims to assess whether a new genetic testing kit which can identify the presence of bacteria and viruses within hours rather than days is a feasible tool in improving antibiotic prescribing and rationalisation of therapy in critically ill children with suspected lower respiratory tract infection.

Interventions

DIAGNOSTIC_TESTRapid Pathogen Detection

Rapid assays for pathogen detection on bronchoalveolar lavage fluid

Sponsors

Cambridge University Hospitals NHS Foundation Trust
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
0 Months to 16 Years
Healthy volunteers
No

Inclusion criteria

1. Aged \>37 weeks corrected gestation and ≤16 years old 2. Receiving mechanical ventilation 3. Commencing or already receiving antibiotic treatment for lower respiratory tract infection

Exclusion criteria

1\. Survival not expected/active medical treatment expected to be withdrawn/palliative care only

Design outcomes

Primary

MeasureTime frameDescription
Performance of the novel pathogen detection assay3 yearsPerformance of novel pathogen detection assays compared to standard microbiology, in regard to sensitivity, specificity and likelihood ratios

Secondary

MeasureTime frameDescription
Time to results3 yearsTime to reportable test results
Negative cultures3 yearsWhere routine culture is negative, what proportion of tests have a positive detection using the novel assay?
Antibiotic therapy3 yearsDuration of therapy and number of antibiotic classes during paediatric intensive care unit admission

Other

MeasureTime frameDescription
Prevalence of COVID19 in children admitted to PICU2 yearsNumber of critically ill children requiring mechanical ventilation with COVID19 compared to those without
Prevalence of SARS-CoV-2 antigen in faecal samples following acute admission with COVID-19 related illness2 yearsFaecal excretion of SARS-CoV-2

Countries

United Kingdom

Contacts

Primary ContactNazima Pathan, FRCPCH PhD
np409@cam.ac.uk01225245151

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026