Developed by Shray Alag, The Harker School
Sections: Correlations,
Clinical Trials, and HPO
Navigate: Clinical Trials and HPO
| Name (Synonyms) | Correlation | |
|---|---|---|
| drug8 | 0.12% Chlorhexidine oral/nasal rinse Wiki | 0.50 |
| drug3508 | Saline oral/nasal rinse Wiki | 0.50 |
| drug23 | 10% Povidone-iodine nasal decolonization swab plus 0.12% CHG oral rinse Wiki | 0.50 |
| Name (Synonyms) | Correlation | |
|---|---|---|
| drug10 | 0.5% Povidone/Iodine oral/nasal rinse Wiki | 0.50 |
| drug21 | 1. Characterize the immune response after infection with SARS-CoV-2 Wiki | 0.50 |
| drug3596 | Serology test for COVID-19 Wiki | 0.35 |
| drug12 | 0.9% Saline Wiki | 0.35 |
| drug4687 | questionnaire Wiki | 0.19 |
| drug274 | Anakinra Wiki | 0.17 |
| drug2575 | No intervention Wiki | 0.10 |
| Name (Synonyms) | Correlation | |
|---|---|---|
| D015658 | HIV Infections NIH | 0.50 |
| D007239 | Infection NIH | 0.07 |
| D003141 | Communicable Diseases NIH | 0.04 |
| Name (Synonyms) | Correlation |
|---|
Navigate: Correlations HPO
There are 4 clinical trials
Currently, limited data is available about patients with HIV in the context of the COVID-19 pandemic. People with HIV who have not achieved viral suppression through antiretroviral treatment may have a compromised immune system that leaves them vulnerable to infections and disease progression. However, little is known about the presentation and clinical outcomes of patients with HIV and SARS-CoV-2. Our aim is to characterize the clinical presentation and disease course of COVID-19 in patients with HIV.
Description: COVID-19 related death among patients with HIV and COVID-19
Measure: Mortality Time: 30 daysDescription: Percentage of patients who required hospitalization
Measure: Frequency of patients requiring hospital admissions Time: 30 daysDescription: Percentage of patients who required ICU admission
Measure: Frequency of patients requiring ICU admissions Time: 30 daysDescription: Percentage of patients who required respiratory support (new oxygen use, non-invasive ventilation,or invasive ventilation)
Measure: Frequency of respiratory support use Time: 30 daysDescription: Percentage of patients who developed acute kidney injury defined as increase in baseline creatinine, or use of renal replacement therapy
Measure: Frequency of kidney injury Time: 30 daysDescription: Percentage of patients who developed liver injury defined as increase in baseline ALT
Measure: Frequency of liver injury Time: 30 daysCOHIVE is an observational cohort nested in four antiretroviral therapy research studies (ADVANCE - NCT03122262; D²EFT - NCT03017872; DolPHIN2 - NCT03249181 and NAMSAL-ANRS12313 - NCT02777229). COHIVE will include participants who are possible COVID-19 cases with symptoms or confirmed COVID-19 cases, and participants who agree to have a serology testing for SARS-CoV-2 regardless of COVID-19 history.
Description: To characterise the clinical features of symptomatic COVID-19 in PLWH (cardio-respiratory and other clinical signs or symptoms), described overall and by HIV and comorbid disease factors including pregnancy status.
Measure: Clinical features of symptomatic COVID-19 in people living with HIV (PLWH) Time: At baselineDescription: To characterise the clinical outcomes of symptomatic COVID-19 in PLWH, assessing the outcomes of patients including the percentage of patients who are fully recovered, required hospitalisation, developed severe illness (ICU admission or equivalent) or died.
Measure: Clinical outcomes of symptomatic COVID-19 in PLWH Time: At Day 28Description: To characterise the clinical outcomes of symptomatic COVID-19 in PLWH, assessing the outcomes of patients including the percentage of patients who are fully recovered, required hospitalisation, developed severe illness (ICU admission or equivalent) or died.
Measure: Clinical outcomes of symptomatic COVID-19 in PLWH Time: At Month 3Description: To determine seroprevalence of COVID-19 in all parent study participants regardless of COVID-19 history.
Measure: Seroprevalence of COVID-19 in all parent study participants Time: Through study completion, an average of one yearThe purpose of the study is to assess seroprevalence of COVID-19 infection in a cohort of HIV + patients and in a cohort of patients taking PrEP by emtricitabine / tenofovir.
Description: % of anti-covid positive cells
Measure: Presence and quantification of CD4 / CD8 reactivity to COVID-19 epitopes in patient with positive and negative serological tests for covid-19 Time: 3 monthsThe non-essential and non-urgent follow-up consultations of patients living with HIV were postponed or transformed into "teleconsultation" or exchanges of e-mails between practitioners and patients during COVID-19 epidemic. This change in care can have an impact on follow-up and access to treatment for PVVIH.
Description: Determination of the number of patients with microbiologically or clinically-biologically proven SARS CoV2 infection at inclusion in the study
Measure: Prevalence of SARS CoV2 infection in PVVIH in Hauts de France Time: InclusionDescription: Determination of the number of patients with microbiologically or clinically-biologically proven SARS CoV2 infection at the end of the study
Measure: Prevalence of SARS CoV2 infection in PVVIH in Hauts de France Time: through study completion, an average of 19 monthsDescription: Percentage of patients who stopped their antiretroviral treatment
Measure: Determine the incidence rate of COVID 19 among PVVIH antiretroviral treatment Time: through study completion, an average of 19 monthsDescription: Reason for discontinuing antiretroviral treatment
Measure: Determine the incidence rate of COVID 19 among PVVIH discontinuing antiretroviral treatment Time: through study completion, an average of 19 monthsDescription: Percentage of patients who stopped all follow-up by an infectious disease specialist
Measure: Determine the incidence rate of COVID 19 among PVVIH who stopped all follow-up Time: through study completion, an average of 19 monthsDescription: Evaluation of the psychological scales HAD on PVVIH
Measure: Psychological consequences of this epidemic among PVVIH : HAD Time: through study completion, an average of 19 monthsDescription: Evaluation of the psychological scales PROQOL-HIV on PVVIH
Measure: Psychological consequences of this epidemic among PVVIH : PROQOL-HIV Time: through study completion, an average of 19 monthsAlphabetical listing of all HPO terms. Navigate: Correlations Clinical Trials
Data processed on September 26, 2020.
An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.
Drug Reports MeSH Reports HPO Reports