COVID-19CONDITIONNCT04389658
Contagiousness and Immunogenicity Status of COVID-19 in Asymptomatic Population (COVID-19 CONDITION)
An observational study of COVID-19, run by Igenomix at 1 site in Spain.
Trial summary
In late December 2019, a new coronavirus strain emerged in China causing coronavirus disease 2019 (COVID-19). Since then, COVID-19 has become a global pandemic outbreak being declared a "public health emergency of international concern" by the International Health Regulations Emergency Committee of the WHO on January… Read more about this study
- Who is it for?
- Any ageHealthy volunteers can take part
- Conditions the study is for
- COVID-19
- How many people
- 1,526 participants
- Where
- 1 siteSpain
- Study dates
- 7 May 2020to 25 Aug 2020
- Phase
- Observational
- 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 Any age
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: Anonymized data produced by Igenomix from previous PCR and ELISA tests of mainly asymptomatic individuals will be used in this study. Approximately, 1,000 cases will be assessed.
Who may be able to join
- Mainly asymptomatic individuals from different corporations of urban areas of Barcelona, Madrid and Valencia that have performed the test before initiating the work immediately after Spanish lockdown from the end of April until beginning of May.
Who cannot join
- There is not exclusion criteria for this study.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Retrospective Observational Study to Determine COVID-19 Contagious and Immunological Status in Asymptomatic Population of Highly Affected Areas
In late December 2019, a new coronavirus strain emerged in China causing coronavirus disease 2019 (COVID-19). Since then, COVID-19 has become a global pandemic outbreak being declared a "public health emergency of international concern" by the International Health Regulations Emergency Committee of the WHO on January 30, 2020. Several emergency measures have been implemented in different countries such as lockdown, social distancing and testing. However, due to the lack of tests worldwide the real number of affected and/or immunized people remains largely unknown. In this moment, when reopening phases are being 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 the severity and time of the pandemic as well as the number of resources available. The present study aims to retrospectively describe the immune and infective spectrum of illness from Severe Acute Respiratory Syndrome Coronavirus 2 (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, right after the lockdown period.
Read the detailed description
In late December 2019, a new coronavirus strain emerged in Chinese megacity Wuhan. The World Health Organization (WHO) named it Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV2) leading to coronavirus disease 2019 (COVID-19). On January 30, 2020 the International Health Regulations Emergency Committee of the WHO declared the outbreak a "public health emergency of international concern". On March 11, 2020 WHO characterized COVID-19 as a pandemic and on March 14th, the Spanish President COVID-19 outbreak a "national emergency" for second time in 40 years.
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
- COVID-19
- Keywords
- SARS-CoV-2, Severe acute respiratory syndrome coronavirus 2, COVID-19
- Medical subject headings
- COVID-19
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| 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. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Prevalence of contagiousness in asymptomatic individuals by PCR
This outcome measure statistically quantifies the Prevalence of contagiousness in asymptomatic individuals based on the gold standard test (PCR).
These results will be analysed in order to focus on the best combination to detect the presence of the disease and the immunological stage in this population at the three main areas of Spain (Madrid, Barcelona and Valencia) with high impact of COVID-19.
Measured: 2 months
Ratio of asymptomatic immunized (IgA/IgM and IgG) population
This outcome measure statistically quantifies the rate of immunized (IgA/IgM and IgG) individuals based on the ELISA test.
These results will be analysed in order to focus on the best combination to detect the presence of the disease and the immunological stage in this population at the three main areas of Spain (Madrid, Barcelona and Valencia) with high impact of COVID-19.
Measured: 2 months
Secondary outcomes (1)
Description of demographic characteristics
Age, gender and location distribution of affected contagious individuals at the three main areas of Spain (Madrid, Barcelona and Valencia) with high impact of COVID-19.
Measured: 2 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 May 2020
- Study start7 May 2020
- Primary completion10 Jun 2020
- Study completion25 Aug 2020
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for COVID-19Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Retrospective
- Enrolment
- 1,526 participants (actual)
Sponsor and investigators
- Lead sponsor
- Igenomix
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Xavier Santamaria, MD,PhD, Principal investigator, IgenomixCarlos Simon, MD,PhD, Principal investigator, Igenomix
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04389658
- Sponsor's protocol ID
- IGX1-COV-XS-20-01
- Acronym
- CONDITION
- Status last verified
- Oct 2020
- First submitted
- 14 May 2020
- Last updated
- 9 Oct 2020
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 9 Oct 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Retrospective Observational Study to Determine COVID-19 Contagious and Immunological Status in Asymptomatic Population of Highly Affected Areas
- ClinicalTrials.gov ID
- NCT04389658
- Acronym / sponsor ID
- CONDITION / IGX1-COV-XS-20-01
- Conditions
- COVID-19
- Keywords
- SARS-CoV-2, Severe acute respiratory syndrome coronavirus 2, COVID-19
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 1,526 participants (actual)
- Lead sponsor
- IgenomixIndustry (pharma, biotech, devices)
- Study start
- 7 May 2020 (actual)
- Primary completion
- 10 Jun 2020 (actual)
- Study completion
- 25 Aug 2020 (actual)
- First posted
- 15 May 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
In late December 2019, a new coronavirus strain emerged in China causing coronavirus disease 2019 (COVID-19). Since then, COVID-19 has become a global pandemic outbreak being declared a "public health emergency of international concern" by the International Health Regulations Emergency Committee of the WHO on January 30, 2020. Several emergency measures have been implemented in different countries such as lockdown, social distancing and testing. However, due to the lack of tests worldwide the real number of affected and/or immunized people remains largely unknown. In this moment, when reopening phases are being 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 the severity and time of the pandemic as well as the number of resources available. The present study aims to retrospectively describe the immune and infective spectrum of illness from Severe Acute Respiratory Syndrome Coronavirus 2 (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, right after the lockdown period.
Detailed description
In late December 2019, a new coronavirus strain emerged in Chinese megacity Wuhan. The World Health Organization (WHO) named it Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV2) leading to coronavirus disease 2019 (COVID-19). On January 30, 2020 the International Health Regulations Emergency Committee of the WHO declared the outbreak a "public health emergency of international concern". On March 11, 2020 WHO characterized COVID-19 as a pandemic and on March 14th, the Spanish President COVID-19 outbreak a "national emergency" for second time in 40 years.
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.
Study design
- Observational model
- Other
- Time perspective
- Retrospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| 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. |
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Anonymized data produced by Igenomix from previous PCR and ELISA tests of mainly asymptomatic individuals will be used in this study. Approximately, 1,000 cases will be assessed.
Key inclusion criteria (1 listed)
- Mainly asymptomatic individuals from different corporations of urban areas of Barcelona, Madrid and Valencia that have performed the test before initiating the work immediately after Spanish lockdown from the end of April until beginning of May.
Key exclusion criteria (1 listed)
- There is not exclusion criteria for this study.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Prevalence of contagiousness in asymptomatic individuals by PCR
Time frame: 2 months
This outcome measure statistically quantifies the Prevalence of contagiousness in asymptomatic individuals based on the gold standard test (PCR). These results will be analysed in order to focus on the best combination to detect the presence of the disease and the immunological stage in this population at the three main areas of Spain (Madrid, Barcelona and Valencia) with high impact of COVID-19.
Ratio of asymptomatic immunized (IgA/IgM and IgG) population
Time frame: 2 months
This outcome measure statistically quantifies the rate of immunized (IgA/IgM and IgG) individuals based on the ELISA test. These results will be analysed in order to focus on the best combination to detect the presence of the disease and the immunological stage in this population at the three main areas of Spain (Madrid, Barcelona and Valencia) with high impact of COVID-19.
1 secondary outcome
Description of demographic characteristics
Time frame: 2 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 9 Oct 2020.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Xavier Santamaria, MD,PhD principal investigator
Igenomix
Carlos Simon, MD,PhD principal investigator
Igenomix
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of COVID-19, run by Igenomix at 1 site in Spain.
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 1 inclusion and 1 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 9 Oct 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 Spain. 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?
Prevalence of contagiousness in asymptomatic individuals by PCR (time frame: 2 months). The study lists 2 primary outcomes in all. 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 9 Oct 2020.