Clinical Evaluation of Rapid Antibody Test for Covid-19

COVID-19 Clinical Trial

— CERAbTc-19  

Official title:

Clinical Evaluation of Rapid Antibody Test for Covid-19

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05298462
• Other study ID #: 56480
• Secondary ID: 283264
• Status: Completed
• Phase: N/A
• Start date: May 17, 2020
• Est. completion date: July 24, 2020

Study information

• Verified date: March 2022
• Source: University of Southampton
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Rapid, accurate diagnosis of Covid-19 would greatly help to improve clinical management of patients presenting with symptoms of possible Covid-19. Currently results of the standard test for the virus take 2-3 days to be reported.

Watford General Hospital has imported rapid antibody tests manufactured by Zuhai Livzon Diagnostics Inc in China and our team would like to evaluate their accuracy and clinical usefulness. The test involves taking a drop of blood from the patient (either from a venous blood sample taken for other blood tests, or from a fingerprick). This is applied to a test strip (similar to a pregnancy test) and two drops of diluent are added. If the patient has antibodies to Covid-19, two lines appear on the test strip (like a positive pregnancy test) whereas if the patient has no antibodies, only one line appears (like a negative pregnancy test). There are two different types of antibody: IgM is produced early in the course of the illness (day 7-14) and then IgG is produced later and continues to be present, probably for months or years. There are two test strips, one for each of these types of antibody.

In this study we aim to evaluate the accuracy of this new test, in three groups of patients. Firstly those with proven Covid-19 and at least 7 days after the onset of their illness. We aim to recruit 200 patients in total: at least 138 patients with 10 or more days of symptoms, plus a subgroup of up to 62 patients with 7-9 days of symptoms (to explore the usefulness of the test earlier in the course of illness). The second group of 250 patients will be those hospital staff who report symptoms possibly caused by Covid-19 and are receiving a standard antibody test.

The third group of patients will be those followed up in a "virtual hospital" for clinically suspected Covid-19 who had never been tested with a standard PCR test.

As we are not sure of the accuracy of the new test, its results will not be used to make decisions about treatment for the patient.

This study will enable us to discover rapidly whether the new test is accurate, and if so we will conduct further studies to assess how it can help to improve management of patients with suspected Covid-19.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 397
• Est. completion date: July 24, 2020
• Est. primary completion date: July 24, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Inpatient or patient in the "virtual hospital" with confirmed Covid-19 infection on PCR OR with history of clinically suspected Covid-19 but no PCR test OR hospital staff with clinical suspicion of past Covid-19 infection.

2. Age 18 or over

3. At least 7 days since onset of symptoms

4. Willing and able to give written informed consent

Exclusion Criteria:

1. Symptom duration <7 days.

2. Lack of written consent

3. Age under 18

Related Conditions & MeSH terms

• COVID-19

Intervention

Diagnostic Test:
• Livzon Rapid Antibody Test for COVID-19
Point-of-care Rapid Antibody Test for COVID-19

Locations

Country	Name	City	State
United Kingdom	Watford General Hospital	Watford	Hertfordshire

Sponsors (2)

Lead Sponsor	Collaborator
University of Southampton	West Hertfordshire Hospitals NHS Trust

Country where clinical trial is conducted

United Kingdom, 

References & Publications (1)

Vancheeswaran R, Willcox ML, Stuart B, Knight M, Kandil H, Barlow A, Patel MH, Stockham J, O'Neill A, Clark TW, Wilkinson T, Little P, Francis N, Griffiths G, Moore M. Accuracy of rapid point-of-care antibody test in patients with suspected or confirmed C — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Sensitivity and Specificity	Sensitivity and specificity compared to standard PCR and/or venous antibody test.	At least 7 days after onset of symptoms

External Links

•   Pre-print