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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT05034978
Other study ID # Protocol HK POCT study
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date March 16, 2021
Est. completion date July 31, 2022

Study information

Verified date February 2023
Source Chinese University of Hong Kong
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the project is to study the feasibility of implementing a novel point-of-care test (POCT) for rapid detection of SARS-CoV-2 infection. A CRISPR-based detection kit would be piloted for testing of suspected SARS-CoV-2 infection in healthcare setting, with the objectives of evaluating the performance of the new test in the detection of SARS-CoV-2, and assessing the practicability of the new test for diagnosing SARS-CoV-2 infection in healthcare settings.


Description:

A CRISPR-based lateral flow assay (LFA) detection kit would be designed and developed for testing for the presence of SARS-CoV-2. The aim of the project is to study the feasibility of implementing the novel point-of-care test (POCT) for rapid detection of SARS-CoV-2 infection in health service setting, with the following objectives: (b) Evaluation of the performance of novel POCT in comparison with conventional quantitative PCR in diagnosis SARS-CoV-2 infection and (c) Assessment of the practicability of LFA-CRISPR-based tests in the operating environments in healthcare settings. Patients who are admitted to the isolation wards of Prince of Wales Hospital, Hong Kong would be invited to join the study. A total of 600 persons with suspected SARS-CoV-2 infection presenting with different symptomatology and epidemiological history will be recruited. Nasal, deep saliva and/or mouth gargle samples will be collected from all recruited subjects in accordance with standard clinical protocol. The samples would be tested for SARS-CoV-2 by the new Point-of-care test, in parallel with standard diagnostic testing of the hospital.


Recruitment information / eligibility

Status Terminated
Enrollment 150
Est. completion date July 31, 2022
Est. primary completion date July 31, 2022
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - adult patients admitted to isolation wards of the hospital who are - of age of 18 or above; - presentation with symptoms of COVID-19 and/or - demonstration of exposure risk to SARS-CoV-2 infection. Exclusion Criteria: - inability to communicate in English or Chinese; - known history of mental illness; - prisoners.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
no intervention
evaluating the performance of a novel point-of-care test

Locations

Country Name City State
Hong Kong Stanley Ho Centre for Emerging Infectious Diseases, The Chinese University of Hong Kong Hong Kong

Sponsors (1)

Lead Sponsor Collaborator
Chinese University of Hong Kong

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type Measure Description Time frame Safety issue
Primary Test performance agreement of point-of-care test result and conventional test 1 year
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