CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


Saliva collectionWiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (7)


Name (Synonyms) Correlation
drug197 Blood collection Wiki 0.71
drug329 Clinical interview Wiki 0.71
drug233 CERC-002 Wiki 0.71
drug210 Blood samples collection Wiki 0.71
drug136 Azithromycin Tablets Wiki 0.50
drug608 Hydroxychloroquine Sulfate Wiki 0.22
drug1016 Placebo Wiki 0.05

Correlated MeSH Terms (7)


Name (Synonyms) Correlation
D014947 Wounds and Injuries NIH 0.20
D055371 Acute Lung Injury NIH 0.17
D055370 Lung Injury NIH 0.16
D012128 Respiratory Distress Syndrome, Adult NIH 0.15
D012127 Respiratory Distress Syndrome, Newborn NIH 0.08
D011014 Pneumonia NIH 0.05
D018352 Coronavirus Infections NIH 0.03

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There are 2 clinical trials

Clinical Trials


1 Human Ab Response & immunoMONItoring of COVID-19 Patients

Prospective, mono centric study on COVID-19 patients with or without acute respiratory distress syndrome (ARDS) to analyse the dynamics of the immune response and to search for biomarkers of evolution

NCT04373200 SARS-CoV-2 Coronavirus Acute Respiratory Distress Syndrome Biological: Blood samples collection Other: Saliva collection
MeSH:Coronavirus Infections Respiratory Distress Syndrome, Newborn Respiratory Distress Syndrome, Adult Acute Lung Injury

Primary Outcomes

Description: Blood sample

Measure: Number of increased immune population

Time: Month 4

Description: Blood sample

Measure: Number of decreased immune population

Time: Month 4

Description: Blood sample

Measure: Number of statically different phenotypes compared to control patients

Time: Month 4

Secondary Outcomes

Description: Qualitative identification of immune subpopulations showing a significant variation compared to controls and quantification of this variation (at D1 and/or D14)

Measure: Gain or loss of functional phenotypic markers between D1 and D14

Time: Day 14

Description: Qualitative identification of immune subpopulations showing a significant variation between acute and mild COVID-19 and quantification of this variation (at D1 and/or D14)

Measure: Gain or loss of functional phenotypic markers between between acute and mild infections

Time: Day 14

Description: Qualitative identification of immune subpopulations showing a significant variation between acute stage and recovery (at 4 months) and quantification of this variation

Measure: Gain or loss of functional phenotypic markers between D1 and month 4

Time: Month 4

Description: Blood sample

Measure: Evaluation of V, D, J gene usage alterations in the immunoglobulin and T cell receptor (TCR) repertoires during ARDS linked to COVID-19

Time: Day 14

Description: Blood sample

Measure: Identification of the Ig classes and of V, D, J sequences of anti-CoV-2 antibodies

Time: Month 4

Description: Blood sample

Measure: Characterization of a new set of human antibodies from patients who have recovered of COVID-19

Time: Month 4

2 Study of Kinetics and Efficacy of the Immune Response Against COVID-19 Among Hospital Staff

COVID-19 is a pathology linked to the SARS-CoV-2 virus, a new virus of the coronaviridae family that emerged in China in December 2019 before rapidly becoming a pandemic according to the WHO on March 11, 2020. The epidemic affected France from February 2020. On February 24, a patient hospitalized at Percy hospital was the cause of a major nosocomial epidemic, potentially responsible for more than 250 symptomatic people in the hospital as of April 6. The outbreak was identified by Percy hospital management on March 16, and barrier measures were immediately put in place. From March 20, a mixed investigation unit set up a chain of nasopharyngeal swabs for Percy hospital staff. A COVID-19 case reporting unit was set up at Percy hospital in response to the identification of the outbreak within the hospital. This unit carried out rapid identification and regular follow-up until the return to work of the staff. Thus all symptomatic patients are identified and the COVID-19 case census cell will follow all Percy hospital staff, including volunteers recruited to deal with the epidemic, throughout the duration of the epidemic. This population, captive by nature, will be one of the few described in the world during this epidemic. Current data on short-, medium- and long-term immunity induced by COVID-19 infection are fragmentary, as is the existence of a large asymptomatic population, making it difficult to cut the chains of transmission in the absence of an effective diagnostic tool. Another important issue is the quality of immunity induced by the infection, as it conditions the future of the pandemic, which could become endemic and recurrent if immunity were not sterilizing. As yet unpublished data in primates show that in the primate model re-infection is not possible in the short term, while patients cured from the Wuhan epidemic seem to be detected again positive for virus shedding. The objective of this study is to characterize the immunity (systemic and local) induced by SARS-Cov-2 infection among Percy hospital staff who are at high risk of contamination even in a period of confinement.

NCT04408001 Sars-CoV2 Other: Clinical interview Biological: Blood collection Biological: Saliva collection

Primary Outcomes

Description: The presence of induced immunity will be identified by an Ig family switch on the first two serologies with a high titre of specific IgG and disappearance of IgM.

Measure: Induced SARS-CoV2 immunity

Time: At day 21 (compared to enrollment [Day 0])

Description: The presence of induced immunity will be identified on serology analysis at 6 months.

Measure: Long-term protection of induced SARS-CoV2 immunity at 6 months

Time: 6 months following enrollment

Description: The presence of induced immunity will be identified on serology analysis at 1 year.

Measure: Long-term protection of induced SARS-CoV2 immunity at 1 year

Time: 1 year following enrollment

Description: Kinetics of anti-SARS-CoV-2 antibodies using ELISA technique on serum samples from enrollment (Day 0) to 1 year after enrollement

Measure: Anti-SARS-CoV2 antibodies kinetics in blood throughout the study

Time: From enrollment (Day 0) to 1 year after enrollement

Description: Kinetics of anti-SARS-CoV-2 antibodies using ELISA technique on saliva samples from enrollment (Day 0) to 1 year after enrollement

Measure: Anti-SARS-CoV2 antibodies kinetics in saliva throughout the study

Time: From enrollment (Day 0) to 1 year after enrollement

Description: Kinetics of serum neutralization against SARS-CoV-2 positive using ELISA technique on serum samples from enrollment (Day 0) to 1 year after enrollement.

Measure: Kinetics of serum neutralization in blood throughout the study

Time: From enrollment (Day 0) to 1 year after enrollement

Secondary Outcomes

Description: Anti-SARS-Cov2 seroprevalence measured in serum samples collected at Day 0.

Measure: Anti-SARS-CoV2 seroprevalence in asymptomatic individuals at Day 0

Time: At enrollment (Day 0)

Description: Anti-SARS-Cov2 seroprevalence measured in serum samples collected at Day 21.

Measure: Anti-SARS-CoV2 seroprevalence in asymptomatic individuals at Day 21

Time: At Day 21


No related HPO nodes (Using clinical trials)