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Serological and PCR Testing for COVID-19

Sponsor: Richmond Research Institute

NCT ID: NCT04404062

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Membrane-based immunoassay kit (diagnostic test), Quantitative antibody Tests (diagnostic test), PCR Test (diagnostic test)
How long the study runs
Study runs about 105 months (dates as stated)
About the drug or intervention
Membrane-based immunoassay kit — diagnostic test: The kit is a qualitative membrane-based immunoassay to detect IgG and IgM antibodies to SARS-CoV-2 in whole blood, serum or plasma specimens. · Quantitative antibody Tests — diagnostic test: Antibody titres will be measured from whole blood samples taken from volunteers. · PCR Test — diagnostic test: PCR tests will be conducted on throat swabs taken from volunteers.
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
5 Years to 70 Years
Who
All
Number of participants
2,500
Started
2020-03-16
Last checked
2026-03

Plain English Summary

What is this study?

  • • Testing a new treatment for covid-19
  • • Clinical study - 2,500 participants
  • • Richmond Research Institute (RRI) is applying existing and new COVID-19 PCR and antibody tests to help develop methodologies which provide fast and accurate results

Who can take part?

  • • Ages 5 Years to 70 Years
  • • Diagnosed with covid-19

Where?

  • • London - Richmond Pharmacology Ltd. 1a Newcomen St, London Bridge

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

Richmond Research Institute (RRI) is applying existing and new COVID-19 PCR and antibody tests to help develop methodologies which provide fast and accurate results. Infection with coronavirus (SARS-CoV-2) is currently a worldwide pandemic and reliable testing for COVID-19 is crucial to understand who is infected and therefore a risk to others by spreading the infection. RRI are currently carrying out the following tests: A. Using a membrane-based immunoassay to detect IgG and IgM antibodies to SARS-CoV-2 in whole blood, serum or plasma specimens helps to assess whether an individual has previously had the virus and is potentially immune B. Polymerase Chain Reaction (PCR) testing using an established method to check for active SARS-CoV-2 infections. C. Quantification of anti-SARS-CoV-2 IgG and IgM antibodies in whole blood samples. The above tests are being used by RRI to follow infections (PCR) and immunity (IgG) in their workforce, as well as their families (including children) and visitors to their site. Collecting this data allows the gathering of epidemiological data on SARS-CoV-2 including incidence, prevalence, information on asymptomatic carriers and efficacy of vaccination. Furthermore, identifying individuals that are infected with SARS-CoV-2 has great potential to improve health outcomes by allowing infected individuals to seek the correct medical treatment as well as self-isolate and reduce transmission.

More detail

This is a screening study to measure symptomatic and asymptomatic carriage of SARS-CoV-2 in trial participants to help facilitate early detection of a second wave of SARS-CoV-2 infections. Specifically, this study aims to determine ; to assess the duration of immunity by assessing the number and speed at which trial participants were infected and cleared the virus with or without symptoms; and to determine the length of symptom onset in those with an active infection; levels of IgG antibodies by demographics (sex, age, ethnicity, and intensity of symptoms). Longitudinal assessment of antibody levels will additionally allow for assessment of the efficacy of any vaccines adminstered. This study also seeks to explore how many people are asymptomatic carriers. In addition, this study aims to help facilitate the development a quantitative laboratory reference test for antibodies (IgG). By using multiple different tests, it can be determined if a person is currently infected with SARS-CoV-2 or whether they previously have been infected. This allows for the scanning of people with asymptomatic carriage of the virus, which is important to help reduce the spread of SARS-CoV-2 through contact with people unaware of infection. Polymerase Chain Reaction (PCR) testing is routinely used to check for active SARS-CoV-2 infections. It measures whether viral RNA is present in an individual's system. All in-house PCR tests are verified by an independent laboratory to check for false positives. Using a membrane-based immunoassay to detect IgG and IgM antibodies to SARS-CoV-2 in whole blood, serum or plasma specimens helps to assess whether an individual has previously had the virus and is potentially immune. IgG and IgM detection components are separate allowing for differential detection of each antibody. To this date, 20904 PCR tests and 6848 antibody tests have been carried out in 2328 individuals, providing some interim data. Of the 20904 PCR tests, 17635 (84%) were negative and 132 (1%) were negative. Of the 6848 antibody tests, 706 (10%) were positive for IgG only, 64 (1%) were positive for IgM only, and 351 (5%) were positive for both IgG and IgM. 5710 (83%) tests were negative. Of those individuals with a positive PCR test, 53% reported fever during the previous two months and 75% reported a loss of taste during the previous two months. Interim results are shown in the medRxiv papers below: https://www.medrxiv.org/content/10.1101/2020.12.08.20245894v2 https://www.medrxiv.org/content/10.1101/2021.04.09.21255200v1

COVID-19

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What we know so far

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 5 Years - 70 Years
  • Who can join: All genders

What the study is looking for

  • ✓Male or female aged 5 to 70 years.
  • ✓An understanding, ability, and willingness to fully comply with the project procedures and restrictions.

Who cannot take part

  • ✗Not applicable.
See the full criteria
Inclusion Criteria: * Male or female aged 5 to 70 years. * An understanding, ability, and willingness to fully comply with the project procedures and restrictions. Exclusion Criteria: * Not applicable.

Where Is This Study? (1 UK site)

Richmond Pharmacology Ltd. 1a Newcomen St, London Bridge

London SE1 1YR, United Kingdom

Recruiting
Site contact (verified)
Jorg Taubel, MD FFPMPrincipal Investigator

How to Get in Touch

Jorg Taubel, MD

Sponsor contact

CONTACT

+44(0)2070425800 j.taubel@richmondpharmacology.com

Ulrike Lorch, MD

Sponsor contact

CONTACT

+44(0)2038482005 u.lorch@richmondpharmacology.com
Data sourced from ClinicalTrials.gov · Last verified: 2026-03