CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


hydroxychloroquineWiki

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


Correlated Drug Terms (5)


Name (Synonyms) Correlation
drug1040 SivoMixx (200 billion) Wiki 0.82
drug1270 azithromycin Wiki 0.58
drug1317 hydroxychloroquine placebo Wiki 0.58
drug808 Oxygen-ozone therapy, probiotic supplementation and Standard of care Wiki 0.58
drug108 Azithromycin Wiki 0.22

Correlated MeSH Terms (6)


Name (Synonyms) Correlation
D003967 Diarrhea NIH 0.58
D011014 Pneumonia NIH 0.09
D011024 Pneumonia, Viral NIH 0.08
D007239 Infection NIH 0.04
D045169 Severe Acute Respiratory Syndrome NIH 0.03
D018352 Coronavirus Infections NIH 0.03

Correlated HPO Terms (2)


Name (Synonyms) Correlation
HP:0002014 Diarrhea HPO 0.58
HP:0002090 Pneumonia HPO 0.09

There are 3 clinical trials

Clinical Trials


1 Randomized Multicenter Study Evaluating the Efficacy of Azithromycin and Hydroxychloroquine in the Prevention of SARS-CoV-2 Infection in the Hospital Population Exposed to Virus

The Investigators propose to set up a preventive trial of infection in hospital workers at risk of coronavirus infection by comparing the rate of SARS-Cov-2 infection in a population of negative SARS-Cov-2 hospital workers receiving preventively azithromycin, hydroxychloroquine or a Placebo

NCT04344379 SARS-CoV-2 Infection Drug: hydroxychloroquine Drug: azithromycin Drug: hydroxychloroquine placebo
MeSH:Infection

Primary Outcomes

Description: The number of hospital workers with a positive serology or a positive PCR within 40 days of follow-up.

Measure: To assess the impact of hydroxychloroquine and azithromycin on the prevention of SARS-CoV-2 contamination in hospital workers exposed to 40 days of treatment.

Time: 3 months

Secondary Outcomes

Description: Clinical signs suggesting SARS-2 CoV infection confirmed by positive endonasal PCR

Measure: Reducing clinical episodes due to suspected SARS-2 CoV infection confirmed by PCR

Time: 40 days

Description: number of seroconversion by serology between Day 0 and Day 40.

Measure: Reducing seroconversion for SARS-CoV-2 without any clinical sign

Time: 3 months

Description: number of cardiological severe adverse events assessed (ECG abnormalities : widening QT, ventricular arythmia, and cardiac arrests), other serious adverse events including hospitalizations, and deaths

Measure: Evaluation of drug tolerance in the study

Time: 40 days

Description: Number of work stoppages over the period

Measure: Evaluation on work stopping of hospital workers

Time: 40 days

Description: Plasmatic concentrations of treatments

Measure: Observance of treatment measured by plasmatic concentrations of hydroxychloroquine or azythromycine

Time: 40 days

Description: number of cardiac events, especialy ECG abnormalities (widening QT) due to treatments

Measure: Incidence of cardiologic events

Time: 40 days

2 Oxygen-Ozone as Adjuvant Treatment in Early Control of Disease Progression in Patients With COVID-19 Associated With Modulation of the Gut Microbial Flora

Italy was the first European country affected by a severe outbreak of the Severe Acute Respiratory Syndrome - CoronaVirus-2 (SARS-CoV-2) epidemic emerged from Wuhan region (China), with a high morbidity and mortality associated with the disease. In light of its pandemic spread and the very limited therapeutic options, COronaVIrus Disease 19 (COVID-19) is considered an unprecedented global health challenge. Therefore, the evaluation of new resources, designed in the first instance for other pathologies but potentially active against COVID-19, represents a priority in clinical research. This is an interventional, non-pharmacological, open, randomized, prospective, non-profit study on the adjuvant use of oxygen ozone therapy plus probiotic supplementation in the early control of disease progression in patients with COVID-19. Contextually, all patients are treated with the current standard of care on the basis of the interim guidelines of the Italian Society of Infectious and Tropical Diseases. The main purpose of the study is to evaluate the effectiveness of an ozone therapy-based intervention (accompanied by supplementation with probiotics) in containing the progression of COVID-19 and in preventing the need for hospitalization in intensive care units.

NCT04366089 COVID SARS-CoV 2 Pneumonia, Viral Coronavirus Infection Other: Oxygen-ozone therapy, probiotic supplementation and Standard of care Dietary Supplement: SivoMixx (200 billion) Drug: Azithromycin Drug: hydroxychloroquine
MeSH:Coronavirus Infections Severe Acute Respiratory Syndrome Pneumonia, Viral Pneumonia
HPO:Pneumonia

Primary Outcomes

Description: Comparison between the two groups

Measure: Delta in the number of patients requiring orotracheal intubation despite treatment

Time: 21 days

Secondary Outcomes

Description: Comparison between the two groups

Measure: Delta of crude mortality

Time: 21 days

Description: Comparison between the two groups

Measure: Delta of length of stay for patients in hospital

Time: 90 days

Description: Comparison between the two groups

Measure: delta in the value of interleukin (IL)-1

Time: 21 days

Description: Comparison between the two groups

Measure: delta in the value of IL-6

Time: 21 days

Description: Comparison between the two groups

Measure: delta in the value of IL-10

Time: 21 days

Description: Comparison between the two groups

Measure: delta in the value of Tumor Necrosis Factor (TNF)-alpha

Time: 21 days

Description: Comparison between the two groups

Measure: delta in the value of cluster of differentiation (CD)4+ CD38/ Human Leukocyte Antigen-DR isotype (HLA-DR)

Time: 21 days

Description: Comparison between the two groups

Measure: delta in the value of CD8+ CD38/ HLA-DR

Time: 21 days

Description: Comparison between the two groups

Measure: delta in the value of fecal calprotectin

Time: 21 days

Description: Comparison between the two groups

Measure: delta in the value of lipopolysaccharide (LPS)

Time: 21 days

Description: Comparison between the two groups

Measure: delta in the value of zonulin

Time: 21 days

Description: Comparison between the two groups

Measure: delta in the value of alpha1-antitrypsin

Time: 21 days

3 Evaluation of the Impact of Bacteriotherapy in the Treatment of COVID-19

In light of its high morbidity and mortality, COronaVIrus Disease 19 (COVID-19) pandemic spread is considered an unprecedented global health challenge. Given the very limited therapeutic options available against Severe Acute Respiratory Syndrome - CoronaVirus-2 (SARS-CoV-2) epidemic at this time, the evaluation of new resources, designed in the first instance for other pathologies but potentially active against COVID-19, represents a priority in clinical research. This is an observational, retrospective, non-profit study on the adjuvant use of bacteriotherapy in the early control of disease progression in patients affected by COVID-19 and treated with the current standard of care on the basis of the interim guidelines of the Italian Society of Infectious and Tropical Diseases. The main purpose of the study is to evaluate the effectiveness of bacteriotherapy in reducing the clinical impact of acute diarrhea, containing the progression of COVID-19 and preventing the need for hospitalization in intensive care units.

NCT04368351 COVID Pneumonia Diarrhea Dietary Supplement: SivoMixx (200 billion) Drug: Azithromycin Drug: hydroxychloroquine
MeSH:Pneumonia Diarrhea
HPO:Diarrhea Pneumonia

Primary Outcomes

Description: Comparison between the two groups. Acute diarrhea was defined as a stool with increased water content, volume, or frequency that lasts less than 14 days.

Measure: delta of time of disappearance of acute diarrhea

Time: 21 days

Secondary Outcomes

Description: Comparison between the two groups

Measure: Delta in the number of patients requiring orotracheal intubation despite treatment

Time: 21 days

Description: Comparison between the two groups

Measure: Delta of crude mortality

Time: 21 days

Description: Comparison between the two groups

Measure: Delta of length of stay for patients in hospital

Time: 21 days


Related HPO nodes (Using clinical trials)


HP:0002014: Diarrhea
Genes 355
MEFV JAK3 IL2RG CD247 NCF4 PIGT IL2RG MYO5B PMM2 GALT JAK3 MYO5B ITGA2 PTEN ABCB4 USP7 CD40LG IGHM HEXB MLYCD SKIV2L TTC37 TMPRSS15 DCLRE1C MC2R ZAP70 KIF1B NOD2 IL6 ABCC8 HSD3B7 PRKN EFL1 SLC12A3 CARMIL2 POLG LRRC8A ANTXR2 ATP8B1 OTULIN SNCA WNT2B MRAP SLC46A1 CHD7 SERPING1 FOXP3 UCP2 IGKC CPOX ABCB11 IRAK1 CD3D DAXX UCHL1 VPS13C SLC9A3 SMAD4 TSHR SCNN1G CD79B DDC DGAT1 SRP54 ANTXR2 SLC12A1 IL7R BMPR1A BMPR1A AKR1D1 SMAD4 SLC39A4 ICOS ADA DNASE1L3 IL7R GATA6 GREM1 ITGB4 EPCAM B2M ALG3 RFX5 ARX LCK ELP1 DCLRE1C CLCNKB SERPING1 EDN3 MVK LIG4 GINS1 TYMP KRAS PALB2 ELANE CASP8 SCNN1A MCM6 CYP11B2 CD79A PODXL CFH SMAD4 SERPING1 HTRA2 LRBA ACADM SLC5A1 NEUROG3 NBN FBP1 BLNK ITGA2B RET RFXAP DCLRE1C ALG8 SLC26A3 RMRP TCF3 C5 TSHR MEN1 PLVAP RECQL4 ACTG2 EDNRB CDKN2B RET GNS SLC10A2 LCT SCNN1B RAG2 DBH ADA EGFR STAT1 TTC37 STAR WAS RFXANK ALDOB IL21R RFXANK SGSH CDKN1A RFX6 POLG KIF23 PARK7 ACSF3 TTR ATP7A ACSF3 RAG1 TTR CIITA IDUA RFXAP ADA DNMT3B RAG2 NLRC4 CR2 BTK C1R GFI1 LIPA IL2RG TNFRSF13C ATRX SON ACVRL1 SKIV2L PIK3R1 SAR1B KCNJ11 SLC46A1 CD55 TERT SLC7A7 MEN1 COG4 SAA1 GDNF ACAT1 NEUROG3 NAXD SCN11A ITCH CD79A CDKN1B GLA RNF113A RAG1 MGME1 SAR1B ETHE1 RAG1 NNT TLK2 GUCY2C BTK TFRC SMAD4 NHLRC2 CD19 KCNJ1 MVK ETHE1 CLMP STAT4 MVK PHKB IL10RA BRCA2 STAT1 CD79B HLA-B MGME1 SLC39A4 WAS IL21 SMARCD2 SEMA3D AK2 ZAP70 TREH GP1BB IL2RA HMGCL TCN2 BLM TNFRSF1A AGA SUGCT TYMP SLC25A13 MYD88 SAMD9 TNFRSF13B LIPA HPS1 COG6 IKZF1 SLC7A7 NOD2 BTK MPI LRRK2 HMBS RFX5 PPP2R5D ITGA6 CFHR1 ICOS BMPR1A LIG4 TXNRD2 ITGB3 CR2 RAG1 PCSK1 SDHD NAGLU RIPK1 OPLAH AIRE CDKN1B DNAJC6 ERCC2 ALAD HYOU1 HGSNAT C1QA TP53 PPP2R5D AP1S1 CYP27A1 RAG2 SEMA3C RECQL4 CFHR3 SCN9A BMPR1A AVP CCDC47 TCIRG1 RAG2 MAOA RRM2B IKBKB CTLA4 DES PINK1 PKP1 NR3C2 CYP7B1 CIITA SI HADH ADAM17 FOXP3 CPT1A G6PC CD3E PALLD COG4 SPP1 CD247 PIK3R1 STX3 HNF1A NAGS TTC7A TTC7A RNF168 ECE1 PLEC APC HNF4A SLC19A2 IFNGR1 CD3D WIPF1 SLC25A13 SPINT2 NRTN NSUN2 TGFB1 POLA1 NBN IGHM CDKN2A MPV17 BLNK IDS IL7R SP110 F5 PTPRC CDKN2C IGLL1 IL2RB BTD HMGCS2 ENG BRCA1 ENG CD109 CYP27A1 GP1BA
Protein Mutations 1
R192G
SNP 0