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COVID-19 Stroke Apical Lung Examination Study

COVID-19 Stroke Apical Lung Examination Study - A Multi-centre Prospective Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04640428
Enrollment
2000
Registered
2020-11-23
Start date
2020-07-10
Completion date
2021-10-31
Last updated
2021-05-27

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

Conditions

Covid19, Stroke, Acute, Stroke Hemorrhagic, Stroke, Ischemic

Keywords

COVID, stroke, CT, CTA

Brief summary

Multi-centre prospective study evaluating computed tomography angiography studies performed for stroke patients as a diagnostic and prognostic imaging biomarker.

Detailed description

Diagnosis of coronavirus disease 2019 (COVID-19) relies on clinical features and reverse-transcriptase polymerase chain reaction (RT-PCR) testing. The latter is constrained by limited sensitivity and a timescale of hours to yield results, with no point-of-care test widely available. A dedicated computed tomography study of the chest is likely to be more sensitive than RT-PCR for COVID-19. Carotid computed tomography angiography (CTA) is a routine acute stroke investigation and includes the lung apices. We aim to assess the lung apices on CTA for ground glass opacification and compare this with COVID-19 RT-PCR test results and clinical outcome measures.

Interventions

None listed

Sponsors

National Institute for Health Research, United Kingdom
CollaboratorOTHER_GOV
King's College Hospital NHS Trust
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

All adult patients presenting with clinical features of acute ischaemic stroke undergoing investigation with computed tomography angiography at presentation.

Exclusion criteria

Poor image quality. No radiologist report available. Computed tomography angiography performed in a non-acute setting.

Design outcomes

Primary

MeasureTime frameDescription
Accuracy of the computed tomography angiography biomarker relative to the COVID-19 RT-PCR test1 monthDefined by sensitivity, specificity, positive and negative predictive values

Secondary

MeasureTime frameDescription
Prognostic value of the computed tomography biomarker1 monthDefined by its relationship with 30 day mortality and modified rankin scale following treatment

Countries

United Kingdom

Contacts

Primary ContactNathan Chan, FRCR
covidsalesresearch@gmail.com+44(0)7508192126
Backup ContactTom Booth, FRCR
thomas.booth@kcl.ac.uk+44(0)2032993279

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026