Immune Biomarkers of Outcome From COVID-19

COVID-19 Clinical Trial

— IBOC  

Official title:

Immune Dysfunction in COVID-19: Investigation of Mechanisms and Identification of Immune Biomarkers of Clinical Outcome

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04436484
• Other study ID #: 20/HEP/381
• Status: Completed
• Start date: April 29, 2020
• Est. completion date: June 14, 2021

Study information

• Verified date: October 2021
• Source: University Hospital Plymouth NHS Trust
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

A new virus to humans, first identified in December 2019, is causing a global pandemic with over 1 million infections and many thousands of deaths. The virus, SARS-CoV2, leads to coronavirus disease 2019 (COVID-19), which mainly affects the breathing system. Around 1 in every 5 people with COVID-19 have more severe infection needing treatment in hospital. Up to half of them require help with breathing in an intensive care unit. Information we have so far about COVID-19 suggests that people with underlying conditions, such as high blood pressure and heart disease, or older people are at higher risk of having severe illness. Scientists do not yet understand why but think it may be related to the immune system.

SARS-CoV2 activates the immune system causing inflammation in the lungs, which is also seen in circulating immune cells in the blood. Preliminary reports show that the response of the immune system can be inappropriate, both overactive and also poorly responsive (exhausted). Changes in the type and function of immune cells have been linked to increased risk of severe disease or death from COVID-19.

In this study, the investigators will look for markers of immune function when a person first attends hospital, which can be used to predict whether they will go on to have a more severe infection. This will help treat patients more effectively, for example, by moving high risk patients to an intensive care setting at an early stage. The team will investigate the immune system in detail in 200 patients with COVID-19 attending University Hospitals Plymouth. The investigators will look for changes in the number, type and function of circulating immune cells and measure whether these changes are linked to severity of the infection or death. The investigators will use established techniques to measure immune function that could be rapidly put into routine hospital care to help guide treatment for individual patients.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 42
• Est. completion date: June 14, 2021
• Est. primary completion date: June 14, 2021
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients attending UHP with COVID-19 infection

• Participants capable of giving informed consent, or if not capable, assent from a personal or nominated consultee

• Age of 18 or over

• Confirmed COVID-19 infection by PCR or antibody testing

Exclusion Criteria:

• Participants on immune suppressing medications within preceding 4 weeks (including systemic corticosteroids with average daily dose equivalent to prednisolone 20 mg)

• Participants on treatment with systemic chemotherapy

• Participants with known immunodeficiency states

• Participants already administered immunomodulating or antiviral agents as part of an interventional trial (this does not include non-specific therapies such as hydroxycholoroquine)

Related Conditions & MeSH terms

• COVID-19

Intervention

Diagnostic Test:
• Peripheral blood sampling
Non-interventional study

Locations

Country	Name	City	State
United Kingdom	University Hospitals Plymouth NHS Trust	Plymouth	Devon

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital Plymouth NHS Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Mortality	Mortality	up to 28 days
Secondary	Mortality	Mortality	Day 4 and Day 10
Secondary	Disease severity	Sequential Organ Failure Assessment (SOFA) score (range 0-24; higher score predicts worse outcome)	Day 4, 10 and 28