CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


TelmisartanWiki

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


Correlated Drug Terms (8)


Name (Synonyms) Correlation
drug2631 Vehicle Control Wiki 0.71
drug2650 Virtual Assistant first, then Human Coach Wiki 0.71
drug2666 Vitamins Wiki 0.71
drug74 APL-9 Wiki 0.71
drug1076 Human Coach first, then Virtual Assistant Wiki 0.71
drug1178 Imatinib Wiki 0.50
drug262 Azithromycin Wiki 0.12
drug1086 Hydroxychloroquine Wiki 0.07

Correlated MeSH Terms (8)


Name (Synonyms) Correlation
D013577 Syndrome NIH 0.08
D045169 Severe Acute Respiratory Syndrome NIH 0.07
D055371 Acute Lung Injury NIH 0.07
D012127 Respiratory Distress Syndrome, Newborn NIH 0.07
D012128 Respiratory Distress Syndrome, Adult NIH 0.06
D003141 Communicable Diseases NIH 0.06
D018352 Coronavirus Infections NIH 0.06
D007239 Infection NIH 0.04

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There are 2 clinical trials

Clinical Trials


1 Outpatient Treatment of Elderly People With Symptomatic SARS-CoV-2 Infection (COVID-19): a Multi-arm, Multi-stage (MAMS) Randomized Trial to Assess the Efficacy and Safety of Several Experimental Treatments to Decrease the Risk of Hospitalization or Death (COVERAGE Trial)

This trial will estimate the efficacy and tolerance of several experimental treatments to prevent hospitalization or death in outpatients aged 60 years or above with Symptomatic SARS-CoV-2 Infection (COVID-19).

NCT04356495 Corona Virus Infection Sars-CoV2 Dietary Supplement: Vitamins Drug: Imatinib Drug: Telmisartan
MeSH:Infection Communicable Diseases Coronavirus Infections Severe Acute Respiratory Syndrome

Primary Outcomes

Measure: Proportion of participants with an occurrence of hospitalization

Time: From inclusion (day0) to day 14

Description: Proportion of participants with an occurrence of death

Measure: Death

Time: From inclusion (day0) to day 14

Secondary Outcomes

Measure: Proportion of hospitalizations, overall and by cause, in each group

Time: From inclusion (day0) to day 28

Description: Proportion of deaths, overall and by cause, in each group

Measure: Death and causes of death

Time: From inclusion (day0) to day 28

Measure: Proportion of intensive care hospitalizations, overall and by cause, in each group

Time: From inclusion (day0) to day 28

Measure: Proportion of participants with negative nasopharyngeal SARS-CoV-2 RT-PCR

Time: day 7 and day 14

Measure: Proportion of participants with a loss of autonomy evaluated by the ADL and IADL scale

Time: day 14 and day 28

Description: Evolution of Haematological markers in each group : Complete Blood Count, prothrombin level, INR

Measure: Haematological markers evolution

Time: from inclusion (day 0) to day 7 and day 14

Description: Evolution of Biochemical markers in each group : ferritin, serum creatinine, urea, sodium, potassium, chlorine, calcium, magnesium, albumin, bicarbonates / tCO2, LDH, CPK, ASAT, ALAT, uricemia

Measure: Biochemical markers evolution

Time: from inclusion (day 0) to day 7 and day 14

Description: Evolution of Inflammatory markers in each group : PCT, CRP

Measure: Inflammatory markers evolution

Time: from inclusion (day 0) to day 7 and day 14

Description: Evolution of immunological markers in each group : B ans T Cells phenotypic profiles

Measure: Immunological markers evolution

Time: from inclusion (day 0) to day 7 and day 14

Description: Number and proportion of grade 1,2,3,4 adverse events in each group

Measure: Adverse events

Time: from inclusion (day 0) to day 14

Description: Number and proportion of grade 1,2,3,4 adverse events in each group

Measure: Adverse reactions

Time: from inclusion (day 0) to day 14

Description: Plasma concentration of the study drugs at D7

Measure: Plasma concentration

Time: day 7

Description: Acceptability of the treatment by participant will be assessed with an interview

Measure: Acceptability of the treatment

Time: from inclusion (day 0) to day 10

2 Efficacy of Hydroxychloroquine, Telmisartan and Azithromycin on the Survival of Hospitalized Elderly Patients With COVID-19: a Randomized, Multicenter, Adaptative Study

In November 2019, Wuhan city in China, became the center of an outbreak of pneumonia due to a novel coronavirus SARS-CoV-2, which disease was named coronavirus disease 2019 (COVID19) in February, 2020. The COVID19 is much more dangerous for people over 60 with a death rate of 3.6% after 60, 8.0% after 70 and 14.8% after 80 -and according to our Italian colleagues over 20% after 90- against 2.3% in the general population. The elderly patients who died most often had multiple comorbidities and in particular: cardiovascular disease (10.5% mortality), diabetes (7.3%), chronic respiratory disease (6.3%) and hypertension (6%). These elderly patients with COVID19 are therefore very fragile and require treatment that fights the virus but is also adapted to their state of health and age. Most of current therapeutic trials worldwide exclude people aged over 75 years, which is precisely the age group affected by COVID19. We therefore propose to carry out a therapeutic trial specific to the elderly with drugs at doses that are bearable for these patients. Using the WHO, clinicaltrial, pubmed and the Chinese CCDC/CHCTR websites to find the better drugs adapted to elderly people, we decided after concertation between infectiologists and geriatricians to do a four arms clinical trial during two weeks twice a day: Hydroxychloroquine 200mg, Telmisartan 40mg, Azithromycin 250mg and standard care. We therefore hypothesize that one or more of these treatments may have a beneficial effect in controlling COVID19, without major and repeated side effects in elderly patients.

NCT04359953 COVID-19 Infection Drug: Hydroxychloroquine Drug: Azithromycin Drug: Telmisartan

Primary Outcomes

Measure: Two-weeks survival rate

Time: Day 14

Secondary Outcomes

Measure: Rate of undetectable RT-PCR of SARS-CoV-2

Time: Day 7

Measure: Rate of undetectable RT-PCR of SARS-CoV-2

Time: Day 14

Measure: Rate of death

Time: Day 28

Measure: Hypotension

Time: Day 7

Measure: Hypotension

Time: Day 14

Measure: Hypothermia and hyperthermia

Time: Day 7

Measure: Hypothermia and hyperthermia

Time: Day 14

Measure: Pneumonia severity according to WHO

Time: Day 7

Measure: Pneumonia severity according to PSI (Hung et al 2017)

Time: Day 7

Measure: Pneumonia severity according to WHO

Time: Day 14

Measure: Pneumonia severity according to PSI (Hung et al 2017)

Time: Day 14

Measure: Rate of no cough

Time: Day 7

Measure: Rate of no cough

Time: Day 14

Measure: Rate of no dyspnea

Time: Day 7

Measure: Rate of no dyspnea

Time: Day 14

Measure: Rate of no fever

Time: Day 7

Measure: Rate of no fever

Time: Day 14

Measure: Rate of no requiring supplemental oxygen

Time: Day 7

Measure: Rate of no requiring supplemental oxygen

Time: Day 14

Measure: Rate of SARS-Cov-2 undetectable

Time: Day 7

Measure: Rate of SARS-Cov-2 undetectable

Time: Day 14

Measure: Recovery time

Time: Day 28

Measure: Critical admission rate

Time: Day 28

Measure: Mechanical ventilation rate

Time: Day 28

Measure: Changes in Activity of Daily Living (ADL) Activity of Daily Living)

Time: Day 13

Measure: Changes in Activity of Daily Living IADL (Instrumental Activity of Daily Living)

Time: Day 13

Measure: The number and dose of added corticosteroids, immonumodulators or immunosuppressants

Time: Day 14


No related HPO nodes (Using clinical trials)