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Corona Virus InfectionROCOCONCT04363593

Serology COVID-19 From the Cornwall Hospital Union

A study testing Serological test and Serum test in people with Corona Virus Infection, run by Centre Hospitalier de Cornouaille at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Coronavirus (COVID-19) is a pandemic-like disease caused by a new coronavirus called Severe Acute Respiratory Syndrome Coronavirus 2 (SARSCoV-2) isolated in China in 2019. Clinical manifestations vary widely from one individual to another, from asymptomatic carrier to a febrile cough that can rapidly lead to acute… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Corona Virus Infection
What is being tested?
Serological test and Serum test
Could I receive a placebo?
No, everyone receives an active treatment
How many people
2,587 participants
Where
1 siteFrance
Study dates
4 May 2020to 16 Nov 2020
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • major
  • having given his or her written consent and being able to consent
  • For the prospective COVID-19 (+) sub-population : Diagnosis of COVID-19 by RT-PCR SARS-CoV-2 (+)
  • For the retrospectiveCOVID-19 (+) sub-population : Serum stored as part of care in patients diagnosed with COVID-19 (+) by an RT-PCR SARS-CoV-2 (+), and no patient opposition obtained.
  • For the prospective COVID-19 (-) sub-population :
  • No suggestive clinical picture associated with RT-PCR SARS-CoV-2 (-) or Evocative clinical picture with RT-PCR SARS-CoV-2 (-) and negative chest CT scan
  • For the retrospective COVID-19 (-) sub-population : Serum kept as part of the care before the outbreak began, and no opposition from the subject obtained.
  • For the staff hospital sub-population : The staff members included must be of legal age, work at the Cornish Hospital Center and have given their written consent and be able to consent.

Who cannot join

  • -Patients with RT-PCR SARS-CoV-2 (-) but with a chest CT suggestive of COVID-19.
  • And for all the patients in different sub-populations :
  • incapable of consent
  • refusal to participate
  • not covered by a social security scheme

Trial locations and contacts

1 site in 1 country.

France1 site
  • CH de Cornouaille

    Quimper, 29000

Other trials in France

About this study

Coronavirus (COVID-19) is a pandemic-like disease caused by a new coronavirus called Severe Acute Respiratory Syndrome Coronavirus 2 (SARSCoV-2) isolated in China in 2019. Clinical manifestations vary widely from one individual to another, from asymptomatic carrier to a febrile cough that can rapidly lead to acute respiratory distress syndrome. Since the beginning of the COVID-19 epidemic, screening by chest X-ray (RT) and polymerase chain reaction (PCR) SARS-CoV-2 conducted by the Cornwall Hospital Union laboratory has shown that among symptomatic patients and hospital staff suspected of being COVID-19, only 7.8% were attributable to COVID-19. Two nosocomial clusters were also identified, in the emergency department (10 carers) and in the cardiology department (6 carers and one patient). However, direct diagnosis by RT-PCR has sensitivity limits and can lead to false negative results when the subject is indeed suffering from COVID-19. This lack of sensitivity is inherent to the technique on the one hand, but also to the quality of the sample and the kinetics of the infection. Indeed, the virological window during which the virus is present in the respiratory mucous membranes sampled seems relatively narrow, hence a progressive negativation of the respiratory samples as the disease progresses. Moreover, clinical symptoms vary from one individual to another, and it is now recognized that some infected persons are asymptomatic but carry the virus. Thus, the use of a second diagnostic technique is a necessity, and serology could be a relevant diagnostic support.

In the literature, several publications report the performance of COVID-19 serology in clusters of cases or cohorts of subjects. The serological techniques employed are variable (target epitopes in particular) and frequently homemade. Serology is mainly studied in comparison or association with RT-PCR in order to highlight the increased performance of COVID-19 diagnosis when the two techniques are combined. Correlation with chest CT imaging data is also encountered.

Numerous serological tests are therefore being tested to determine retrospectively whether the individual has been exposed to the virus by looking for specific antibodies to the virus. The supreme health authority has drawn up specifications dated 16 April 2020, defining the methods for evaluating the performance of serological tests detecting antibodies directed against SARSCoV-2 in order to provide a framework for these practices. Several clinical studies are also underway, in particular to assess the kinetics of the appearance of the antibodies, whether these specific antibodies would be protective and whether their appearance would coincide with a cessation of contagiousness. Thus, the main objective of this study is to evaluate the diagnostic performance of the COVID-19 immunoglobulin (IgG) Dia-Pro serological test, in view of its deployment at the Cornish Hospital Union Laboratory. Subsequently, given the low prevalence of COVID-19 in Brittany and the risk of a second epidemic wave when the confinement is lifted, the evaluation of the seroprevalence of the staff of the Cornish Hospital Union is necessary in order to assess the attack rate of COVID-19 within the establishment and particularly within departments where nosocomial clusters have been reported; and to prevent the impact of deconfinement. Indeed, knowledge of the proportion of immunized personnel and its distribution according to services will make it possible to establish internal recommendations and to effectively manage personal protective equipment inventories, in conjunction with the deconfinement strategy that will be implemented by the government. The goal is to protect hospital staff from overexposure to the virus;

Being tested
Serological test, Serum test
Keywords
coronavirus infection, serology
Medical subject headings
Coronavirus Infections

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Serological testBiological

    Serological testing is performed for patients with confirmed COVID-19 infection by RT-PCR.

  • Serum testBiological

    Use of the serum taken from patients consulted for suspicion of COVID-19 before the beginning of the trial

Study groups in NCT04363593
Study groupRoleWhat they receive
prospective group COVIDOtherNew patients consulting for suspected or diagnosed COVID(+)
Receives: Biological: Serological test
retrospective group COVIDOtherPatients already diagnosed with COVID(+) or with a suspicion of unconfirmed COVID or at a date before the apparition of the COVID infection (April-March 2019)
Receives: Biological: Serum test
Hospital staffOtherAll hospital staff including those already diagnosed at COVID(+)
Receives: Biological: Serological test; Biological: Serum test

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Serological test evaluation

    The performance of the COVID-19 IgG Dia-Pro serological test is evaluated in terms of sensitivity/specificity.

    Measured: 1 day

Secondary outcomes (1)
  1. Population seroprevalence

    Population seroprevalence among hospital staff (caregivers and non-caregivers) in Quimper Hospital is assessed

    Measured: 1 month

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Apr 2020
  2. Study start4 May 2020
  3. Primary completion16 Nov 2020
  4. Study completion16 Nov 2020

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
2,587 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04363593
Sponsor's protocol ID
29BRC20.0122
Acronym
ROCOCO
Status last verified
Dec 2020
First submitted
24 Apr 2020
Last updated
10 Dec 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Serological test and Serum test in people with Corona Virus Infection, run by Centre Hospitalier de Cornouaille at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 10 Dec 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Serological test evaluation (time frame: 1 day). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Dec 2020.

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