Contagiousness and Immunogenicity Status of COVID-19 in Asymptomatic Population (COVID-19 CONDITION)
NCT ID: NCT04389658
Last Updated: 2020-10-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
1526 participants
OBSERVATIONAL
2020-05-07
2020-08-25
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
COVID-19 Contact Study by Antigen Detection Test
NCT04745533
Prevalence and Risk Factors of SARS-CoV-2 Antibody Responses (COVID-19)
NCT04425759
COVID-EC Study: Clinical Characteristics of Patients With COVID-19 in Guayaquil, Ecuador
NCT04362969
Study of the SARS-COV-2 (COVID-19) Serological Profile of an Army Training Hospital Staff
NCT04387838
COVID-19 Among Healthcare Workers in Belgian Hospitals
NCT04373889
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
In order to fight this unanticipated pandemic, emergency measures have been implemented in different countries such as lockdown, social distancing and testing. Massive community testing to detect early or asymptomatic infections as well as social distancing has been used in certain countries (South Korea, Iceland, etc..) with relatively success. In this sense, Polymerase Chain Reaction (PCR) is considered to be the gold standard to diagnose the infection with SARS-CoV2. On the other hand, Enzyme Linked ImmunoAssay (ELISA) has also been widely used to determine the presence of antibodies (Immunoglobulins M, A and G) and, hence immunological status. Some studies have reported the presence of IgM and IgA antibodies within the first 5 days of clinical symptom onset, while IgG is usually detected on 14 days after symptom onset, with a positive rate of 85.4%, 92.7% and 77.9%, respectively. Moreover, a recent report of reveals that positive detection rate is significantly increased when combined IgM/IgA ELISA assay with PCR for each patient compare with a single quantitative PCR test. In this sense Igenomix has recently obtained the authorisation by the Valencia Community Authority to provide these services after completing the requested process of verification.
In this moment, when reopening phases are planning or even undertaken in the majority of countries, the decision to enact any of these measures rests with the judgement of each health care system. However, every country or individual community circumstances may be unique and require contextual consideration based on three main factors: the severity of the pandemic spread, the measures and timing implemented during the pandemic, and the moment of the post pandemic that this population is in. Therefore, international metrics are urged to guide the re-opening of the post pandemic era in different parts of the world to provide a logical approach to mitigate risk to new outbreaks.
This is a retrospective, observational study in which anonymized data from subjects who already performed PCR and ELISA test for COVID-19 detection at Igenomix, will be used to assess the rate of immunized population as well as the rate of asymptomatic contagious population in three hot spots of Spain (Madrid, Barcelona and Valencia) immediately after the lockdown period. After data collection and processing, once the full anonymization process has been completed, the pool of data will be analyzed with the aim of retrospectively describe the immune and infective spectrum of illness from SARS-CoV-2 infection in the general asymptomatic population in three main areas of Spain (Madrid, Barcelona and Valencia) with high impact of COVID-19. Moreover, other additional descriptive variables such as age, gender, etc will be assessed.
Being an observational retrospective study, the sample size would consist of the complete database of individuals analyzed by ELISA and PCR from areas of Madrid, Barcelona and Valencia representing approximately 1,000 cases. Waiver of informed consent form has been duly authorized by the Ethic Committee in agreement to the local legislation.
No intervention involving patients or their biological material will be required.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
OTHER
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Asymptomatic population
Subjects who underwent PCR and ELISA tests for the diagnosis of COVID-19: mainly asymptomatic individuals from three main areas of Spain (Madrid, Barcelona and Valencia) with high impact of COVID-19 that have performed the PCR and ELISA test for the diagnosis of COVID-19 before initiating the work immediately after Spanish lockdown.
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Igenomix
INDUSTRY
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Xavier Santamaria, MD,PhD
Role: PRINCIPAL_INVESTIGATOR
Igenomix
Carlos Simon, MD,PhD
Role: PRINCIPAL_INVESTIGATOR
Igenomix
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Igenomix
Paterna, Valencia, Spain
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
IGX1-COV-XS-20-01
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.