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D000163: Acquired Immunodeficiency Syndrome

Developed by Shray Alag, The Harker School
Sections: Correlations, Clinical Trials, and HPO

Correlations computed by analyzing all clinical trials.

Navigate: Clinical Trials and HPO


Correlated Drug Terms (11)


Name (Synonyms) Correlation
drug11 0.5% Povidone/Iodine oral/nasal rinse Wiki 0.50
drug9 0.12% Chlorhexidine oral/nasal rinse Wiki 0.50
drug12 0.9% (w/v) saline Wiki 0.50
Name (Synonyms) Correlation
drug2991 Saline oral/nasal rinse Wiki 0.50
drug22 1. Characterize the immune response after infection with SARS-CoV-2 Wiki 0.50
drug3075 Serology test for COVID-19 Wiki 0.35
drug14 0.9% Saline Wiki 0.35
drug128 AZD1222 Wiki 0.22
drug4037 questionnaire Wiki 0.17
drug210 Anakinra Wiki 0.15
drug2215 No intervention Wiki 0.10

Correlated MeSH Terms (5)


Name (Synonyms) Correlation
D015658 HIV Infections NIH 0.89
D007239 Infection NIH 0.07
D003141 Communicable Diseases NIH 0.04
Name (Synonyms) Correlation
D045169 Severe Acute Respiratory Syndrome NIH 0.02
D018352 Coronavirus Infections NIH 0.02

Correlated HPO Terms (0)


Name (Synonyms) Correlation

Clinical Trials

Navigate: Correlations   HPO

There are 4 clinical trials


1 Prospective Observational Study for Patients With HIV and Confirmed SARS-CoV-2

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.

NCT04333953
Conditions
  1. HIV/AIDS
  2. COVID-19
  3. SARS-CoV-2
Interventions
  1. Other: No intervention
MeSH:Acquired Immunodeficiency Syndrome HIV Infections

Primary Outcomes

Description: COVID-19 related death among patients with HIV and COVID-19

Measure: Mortality

Time: 30 days

Secondary Outcomes

Description: Percentage of patients who required hospitalization

Measure: Frequency of patients requiring hospital admissions

Time: 30 days

Description: Percentage of patients who required ICU admission

Measure: Frequency of patients requiring ICU admissions

Time: 30 days

Description: Percentage of patients who required respiratory support (new oxygen use, non-invasive ventilation,or invasive ventilation)

Measure: Frequency of respiratory support use

Time: 30 days

Description: 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 days

Description: Percentage of patients who developed liver injury defined as increase in baseline ALT

Measure: Frequency of liver injury

Time: 30 days
2 COVID-19 in People Living With HIV: Evaluation of Risk Factors and Outcomes in Resource-limited Settings. A Pooled Substudy of ADVANCE, D²EFT, DolPHIN2 and NAMSAL

COHIVE 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.

NCT04371835
Conditions
  1. HIV-infection/Aids
  2. Coronavirus Infection
MeSH:Infection Communicable Diseases HIV Infections Coronavirus Infections Severe Acute Respiratory Syndrome Acquired Immunodeficiency Syndrome

Primary Outcomes

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 baseline

Description: 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 28

Description: 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 3

Secondary Outcomes

Description: 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 year
3 Prevalence of COVID-19 Infection in a Cohort of Patient Infected by the HIV and Patients Taking PrEP Pre-exposure Prophylaxis

The 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.

NCT04575545
Conditions
  1. Covid19
  2. Virus-HIV
Interventions
  1. Diagnostic Test: Serology test for COVID-19
MeSH:Infection Acquired Immunodeficiency Syndrome HIV Infections

Primary Outcomes

Measure: % of patients with positive serological tests for covid-19

Time: 3 months

Secondary Outcomes

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 months
4 Evaluation of the Impact of the Epidemic of COVID-19 Infection Among People Living With HIV (SARS-CoV-2)

The 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.

NCT04581746
Conditions
  1. Virus-HIV
  2. Covid19
Interventions
  1. Other: questionnaire
MeSH:Infection Acquired Immunodeficiency Syndrome HIV Infections

Primary Outcomes

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: Inclusion

Secondary Outcomes

Description: 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 months

Description: 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 months

Description: 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 months

Description: 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 months

Description: 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 months

Description: 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 months

HPO Nodes


HPO

Alphabetical listing of all HPO terms. Navigate: Correlations   Clinical Trials


HPO Nodes


Reports

Data processed on January 01, 2021.

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  

Interventions

4,818 reports on interventions/drugs

MeSH

706 reports on MeSH terms

HPO

306 reports on HPO terms

All Terms

Alphabetical index of all Terms

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