CovidResearchTrials by Shray Alag

CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)

CT-scanWiki

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


Correlated Drug Terms (6)

Name (Synonyms) Correlation
drug453 EP Wiki 1.00
drug324 Clevudine Wiki 1.00
drug451 EEG Wiki 1.00
drug1094 Pulse oximetry Wiki 1.00
drug213 Blood tests Wiki 0.71
drug591 Hydroxychloroquine Wiki 0.11

Correlated MeSH Terms (1)

Name (Synonyms) Correlation
D001927 Brain Diseases NIH 0.58

Correlated HPO Terms (0)

Name (Synonyms) Correlation

There is one clinical trial.

Clinical Trials

1 Determination of Acute Encephalopathy Predictors in Patients With COVID-19

The SARS-CoV-2 infection was detected in December 2019 in Wuhan City, China. The infection affects all age groups, although childhood is the lowest proportion of those affected. The main clinical manifestations that require hospitalization of infected patients are SARS pneumonia, which may require treatment in the intensive care unit (27%) and its progression into acute respiratory distress syndrome (67%) with life-threatening conditions in almost 25% of patients diagnosed with "SARS-CoV-2 infection". Nervous system damage with SARS-CoV-2 infection has been practically not investigated, but neurological disorders have been reported in 36% of these patients. Finally, the mortality rate associated with the new virus is high in patients who require treatment in intensive care units (62% of cases). Therefore, we are conducting a prospective study to identify acute encephalopathy predictors in patients with COVID-19.

NCT04405544 Encephalopathy COVID Diagnostic Test: CT-scan Diagnostic Test: EEG Diagnostic Test: EP Diagnostic Test: Pulse oximetry Diagnostic Test: Blood tests
MeSH:Brain Diseases
HPO:Encephalopathy

Primary Outcomes

Description: The percentage of patients who have developed encephalopathy

Measure: The percentage of patients who have developed encephalopathy

Time: 10 days

Related HPO nodes (Using clinical trials)

HP:0001298: Encephalopathy
Genes 334
ACTL6B SLC19A3 GABRA1 TH RNASEH2C CACNA1B NDUFA6 SYNJ1 TRAK1 COG8 NDUFAF4 KYNU ND5 CLTC PNKP TCF4 TRNS2 ND2 TRAK1 SLC2A1 FGF12 KCNB1 CNTNAP2 NDUFAF1 PPP3CA MAPK10 CACNA1E TK2 PNPO SLC12A3 KCNQ5 COX3 SPTAN1 TP53 NAXE NDUFV2 BSCL2 RANBP2 TRNS1 GABRG2 NADK2 SLC1A2 MST1 GCDH TRNF DHDDS SLC6A9 KCNA2 GABRB3 SLC25A22 GRIN2B GNAO1 CHD2 ARHGEF9 FBXL4 KCNQ2 NDUFS4 SUCLG1 CAD ZNHIT3 NDUFS3 ACAD9 SLC19A3 LYRM7 SCN1B NEUROD2 PRNP TRNW CYTB CCDC88A SCN9A NDUFA6 DNM1 NDUFS1 KMT2E RANBP2 CLCNKB ACY1 DPM2 DENND5A ALG9 COX15 ITPA SLC35A1 SLC35A2 NDUFS6 GABRB2 TBCD HADH NDUFAF3 STAG1 ATP1A3 RNF13 TBCE GPT2 NDUFV1 ATP5F1D PARS2 CACNA1A SERPINI1 GLYCTK NDUFA11 ST3GAL3 NRXN1 KYNU NRXN1 TMEM126B LIAS CACNA1A ASNS ATP5F1A NDUFS3 COG8 ND1 TBCE PCCB UNC80 FCSK DNM1 ATP5F1A ARX HTRA1 SZT2 DGUOK MDH2 MDM2 TBC1D24 ND3 TBCK GABRB2 TIMMDC1 AP3B2 ADAM22 NTRK2 CPT2 GABRA5 TRIT1 NDUFAF5 KCNQ2 SLC25A22 SYNGAP1 NDUFS7 WDR45 NDUFS2 NUS1 ACSF3 SLC25A20 SCN1A SCN3A GABRB3 KCNA2 CHD2 SLC1A2 COX2 GCDH AARS1 PCK1 IBA57 COQ2 NDUFS8 COQ4 ND1 STAT2 TRNK EEF1A2 MPC1 SLC25A15 SLC13A5 KCNT2 ATP6V1A HCN1 DLD CACNA1B PIGP GRIN2D ROGDI PNPO ATAD1 CUX2 TRNV NDUFAF2 BSCL2 NDUFB10 UBA5 NAXD PHACTR1 LIPT2 GABRB1 NDUFS6 RNASEH2B ETHE1 CDKL5 NDUFAF4 TRNL1 CLCN4 GBA ACY1 AMACR PPP3CA TIMM50 HCN1 TCF4 NDUFB3 NDUFS4 ETHE1 NDUFB11 DLD SZT2 TUFM SH2D1A KCNT1 SLC22A5 GLUL GBA HMGCL TSFM BCS1L AP2M1 CNPY3 CARS2 KCNB1 FADD SYNGAP1 STXBP1 DNM1 SLC25A13 CLP1 PCCA TMEM70 HNRNPU PACS2 FRRS1L CHEK2 NECAP1 D2HGDH MEF2C EEF1A2 SLC6A1 YWHAG NBAS GPR35 COQ9 AP3B2 DHDDS PNPT1 TRNQ SLC25A12 UBA5 CNKSR2 FGF12 GUF1 SIK1 DNM1L NUBPL SUCLA2 GLS NUS1 ARHGEF9 COX1 ARV1 ARV1 NDUFA11 TBC1D24 PLCB1 DOCK7 HIBCH GABRG2 NDUFAF2 SLC25A15 WWOX CARS2 GCSH SYNJ1 NDUFV2 SCN8A ATP6V1A SLC22A5 SLC13A5 NDUFB9 HADH STXBP1 CPT1A TRAPPC12 BOLA3 XIAP FOXRED1 SIK1 SERAC1 NDUFS7 NAGS PIGA PARS2 CYC1 ACAD9 FADD CYFIP2 AARS1 TREX1 PMPCB MECP2 NTRK2 NDUFAF1 TWNK TGFB1 ND6 GRIN1 SLC25A1 SCN2A NDUFB3 CHD2 GRIN2D SCN3A UGT1A1 CLPB NADK2 GLDC CACNA2D2 SCN8A KCNA2 TSEN54 CPLX1 SCN1A NDUFA1 AMT NECAP1 WWOX FBLN1 GABBR2 CDKN2A TRNC TRNK CUX2 GABRA2 CYFIP2
Protein Mutations 1
A3243G
SNP 0