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Serology COVID-19 From the Cornwall Hospital Union (ROCOCO)

Primary Purpose

Corona Virus Infection

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Serological test
Serum test
Sponsored by
Centre Hospitalier de Cornouaille
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Corona Virus Infection focused on measuring coronavirus infection, serology

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 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.

Exclusion Criteria:

-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

Sites / Locations

  • CH de Cornouaille

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Other

Other

Other

Arm Label

prospective group COVID

retrospective group COVID

Hospital staff

Arm Description

New patients consulting for suspected or diagnosed COVID(+)

Patients 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)

All hospital staff including those already diagnosed at COVID(+)

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

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

Full Information

First Posted
April 24, 2020
Last Updated
December 9, 2020
Sponsor
Centre Hospitalier de Cornouaille
Collaborators
Centre Hospitalier Régional et Universitaire de Brest
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1. Study Identification

Unique Protocol Identification Number
NCT04363593
Brief Title
Serology COVID-19 From the Cornwall Hospital Union
Acronym
ROCOCO
Official Title
Serology COVID-19 From the Cornwall Hospital Union
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Completed
Study Start Date
May 4, 2020 (Actual)
Primary Completion Date
November 16, 2020 (Actual)
Study Completion Date
November 16, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier de Cornouaille
Collaborators
Centre Hospitalier Régional et Universitaire de Brest

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief 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 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;

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Corona Virus Infection
Keywords
coronavirus infection, serology

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
2587 (Actual)

8. Arms, Groups, and Interventions

Arm Title
prospective group COVID
Arm Type
Other
Arm Description
New patients consulting for suspected or diagnosed COVID(+)
Arm Title
retrospective group COVID
Arm Type
Other
Arm Description
Patients 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)
Arm Title
Hospital staff
Arm Type
Other
Arm Description
All hospital staff including those already diagnosed at COVID(+)
Intervention Type
Biological
Intervention Name(s)
Serological test
Intervention Description
Serological testing is performed for patients with confirmed COVID-19 infection by RT-PCR.
Intervention Type
Biological
Intervention Name(s)
Serum test
Intervention Description
Use of the serum taken from patients consulted for suspicion of COVID-19 before the beginning of the trial
Primary Outcome Measure Information:
Title
Serological test evaluation
Description
The performance of the COVID-19 IgG Dia-Pro serological test is evaluated in terms of sensitivity/specificity.
Time Frame
1 day
Secondary Outcome Measure Information:
Title
Population seroprevalence
Description
Population seroprevalence among hospital staff (caregivers and non-caregivers) in Quimper Hospital is assessed
Time Frame
1 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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. Exclusion Criteria: -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
Facility Information:
Facility Name
CH de Cornouaille
City
Quimper
ZIP/Postal Code
29000
Country
France

12. IPD Sharing Statement

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Serology COVID-19 From the Cornwall Hospital Union

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