CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


Report for D001927: Brain Diseases NIH

(Synonyms: Brain Diseases)

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


Correlated Drug Terms (5)


Name (Synonyms) Correlation
drug175 Caption AI Wiki 0.71
drug173 Canakinumab Injection 600mg Wiki 0.71
drug172 Canakinumab Injection 300mg Wiki 0.71
drug313 Follow up Wiki 0.50
drug632 Placebos Wiki 0.19

Correlated MeSH Terms (3)


Name (Synonyms) Correlation
D020196 Trauma, Nervous System NIH 0.71
D003693 Delirium NIH 0.50
D016638 Critical Illness NIH 0.37

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There are 2 clinical trials

Clinical Trials


1 Outcomes in Patients With Acute Encephalopathy and SARS-Cov-2 Infection

Infection with SARS-CoV-2 or severe acute respiratory syndrome coronarvirus type 2 was highlighted in December 2019 in the city of Wuhan in China, responsible for an pandemic evolution since March 11, 2020. The infection affects all ages of life, although affecting children in a very small proportion of cases. The typical presentation of the disease combines fever (98%), cough (76%), myalgia and asthenia (18%) as well as leukopenia (25%) and lymphopenia (63%). Upper airway involvement rare. The main clinical presentation requiring hospitalization of infected patients is that of atypical pneumonia which may require critical care management (27%), and progress to an acute respiratory distress syndrome (67%) involving life-threatening conditions in almost 25% of patients diagnosed with SARS-CoV-2 infection. Other organ damage have been reported, mainly concerning kidney damage (29%) which may require renal replacement therapy in approximately 17% of patients. Neurological damage has been very rarely studied, yet reported in 36% of cases in a study including patients of varying severity. Finally, the mortality associated with this emerging virus is high in patients for whom critical care management is necessary, reported in 62% of patients. We therefore propose a prospective observational study which aim at reporting the prevalence of acute encephalopathy at initial management in Critical/Intensive care or Neurocritical care , to report its morbidity and mortality and to identify prognostic factors.

NCT04320472 COVID-19 Encephalopathy Critically Ill Other: Follow up
MeSH:Brain Diseases Critical Illness
HPO:Encephalopathy

Primary Outcomes

Description: ratio of patients with acute encephalopathy among the total of patients with SARS-Cov-2 infection at Critical/Intensive care or Neurocritical care admission

Measure: prevalence

Time: at Critical/Intensive care or Neurocritical care admission

Secondary Outcomes

Description: A favorable outcome is defined by a Glasgow Outcome Scale (GOS) of 5. The Glasgow Outcome Scale (GOS) will be determined patients charts review and/or general practitioner interview conducted by an independent assessor. The GOS score : [1: Death, 2: Persistent vegetative state, 3: Severe disability, 4: Moderate disability, 5 : Low disability]

Measure: Favorable outcome

Time: 3 months

2 Biomarker-guided Assessment of Neurocognitive Impairment in Patients With COVID-19 - a Multicenter Case-control Study

Delirium and acute neurocognitive impairment are increasingly observed in adult and pediatric patients with COVID-19. Prospective clinical studies combining clinical and laboratory examinations including specific biomarkers of neuroaxonal injury were not performed for COVID-19. The value of biomarkers of neuroaxonal injury was proven in preliminary studies. These biomarkers could thus contribute to the systematic detection of neurocognitive impairment in patients with COVID-19. Due to worldwide increasing numbers of hospitalized patients with COVID-19, biomarkers of neuroaxonal injury are highly valuable to detect and monitor cognitive impairment, especially with regard to limited resources available to perform time-consuming brain imaging. Biomarkers of neuroaxonal injury are therefore not only of great interest to detect neurocognitive impairment but also to quantify the severity of brain injury in patients with COVID-19.

NCT04359914 Critical Illness COVID-19 Central Nervous System Injury Delirium Encephalopathy
MeSH:Delirium Brain Diseases Trauma, Nervous System Critical Illness
HPO:Encephalopathy

Primary Outcomes

Description: Assessment of neurocognitive impairment using validated tools

Measure: Incidence of delirium/neurocognitive impairment in adult and pediatric patients with COVID-19 compared to patients without COVID-19

Time: Day 90

Description: Measurement of biomarker levels (e.g. NSE, S100B, neurofilament proteins) derived from blood samples

Measure: Change in neuroaxonal injury biomarker levels in patients with COVID-19 compared to patients without COVID-19

Time: Change from baseline biomarker levels at day 28

Description: Assessment of the neurocognitive performance of patients using validated tests (e.g. Short Blessed Test)

Measure: Neurocognitive 3-months outcome in patients with COVID-19 compared to patients without COVID-19

Time: Day 90

Description: Assessment of the change in the neurocognitive performance of patients using validated tests (e.g. IQCODE)

Measure: Neurocognitive 3-months outcome in patients with COVID-19 compared to patients without COVID-19

Time: Change from baseline IQCODE results at day 90

Secondary Outcomes

Description: Assessment of the overall quality of life using validated tests [e.g. Modified Rankin Scale with a range from 0 (no symptoms) to 6 (dead)]

Measure: Quality of life in patients with COVID-19 compared to patients without COVID-19 after hospital discharge

Time: Day 90

Description: Cumulative days in hospital

Measure: Length of hospital stay in patients with COVID-19 compared to patients without COVID-19

Time: 1 year

Description: Survival after 90 days

Measure: 90-day survival in patients with COVID-19 compared to patients without COVID-19

Time: Day 90


HPO Nodes


HP:0001298: Encephalopathy
Genes 332
ACY1 SCN9A KCNQ2 RANBP2 SIK1 DHDDS NDUFA1 CLPB WDR45 NDUFB3 SCN8A CUX2 SCN1A SLC35A1 SLC6A1 ND1 KCNA2 SLC25A15 ACAD9 TRNS1 KCNB1 PARS2 TSEN54 TMEM70 NDUFV2 GABRB3 UBA5 SLC2A1 BSCL2 SLC25A13 CLCN4 SCN3A GABRA2 NDUFS6 NDUFAF4 COX2 CPT1A SCN1A PCK1 NUBPL COQ2 TIMM50 NDUFB10 FGF12 YWHAG IBA57 TGFB1 TRNQ GRIN1 SLC25A20 NADK2 HMGCL UBA5 CACNA2D2 NECAP1 DOCK7 TRIT1 ND6 NBAS GABBR2 CDKN2A SCN3A SUCLG1 NAXE LYRM7 TRAK1 DNM1L KCNQ5 NDUFAF5 TREX1 TRNK NAXD COX15 DENND5A CHEK2 TBC1D24 GABRG2 TRNV NDUFV2 COX3 DNM1 GABRB3 SLC25A12 GLS GCDH GPR35 PCCB NADK2 NDUFA11 ATP5F1A CACNA1E NDUFAF4 CYFIP2 GRIN2D GBA UGT1A1 ALG9 DNM1 NUS1 RNASEH2C MDM2 COG8 TRNW NRXN1 COQ4 FBXL4 RANBP2 SCN1B PARS2 NDUFS2 GNAO1 SLC22A5 NDUFS7 KCNT1 SERAC1 TBC1D24 BOLA3 LIPT2 WWOX MPC1 GBA PIGP HCN1 CYTB CCDC88A PNKP KMT2E PPP3CA GRIN2D SLC1A2 ETHE1 SLC25A22 TBCK ROGDI BSCL2 STXBP1 TCF4 SLC22A5 NTRK2 SLC19A3 AP2M1 ATP6V1A KCNT2 AP3B2 MST1 COG8 NDUFV1 STXBP1 SLC25A22 TSFM KYNU GRIN2B COX1 HADH ARV1 ATAD1 CYFIP2 CDKL5 TRNF NDUFB11 GABRG2 GPT2 NDUFA11 ATP1A3 TWNK NAGS TRAPPC12 SLC13A5 DLD CPT2 TK2 ATP5F1D CACNA1B ATP5F1A AARS1 RNF13 TRNS2 FCSK FADD PRNP ASNS PHACTR1 NDUFS7 DHDDS AP3B2 ITPA SLC19A3 NDUFAF3 EEF1A2 ARX BCS1L CACNA1A TRNK SLC25A15 PNPO ARV1 ND2 CYC1 NDUFS1 PLCB1 GLYCTK ACY1 CACNA1B XIAP ARHGEF9 NDUFAF2 ND1 NDUFS4 ACAD9 NEUROD2 ADAM22 SLC13A5 COQ9 SLC25A1 PACS2 SZT2 CHD2 NDUFA6 CLP1 CARS2 CARS2 FADD MEF2C NDUFA6 CAD NDUFAF1 GCSH AARS1 TRAK1 MDH2 SYNGAP1 CHD2 HCN1 CACNA1A NDUFS3 SERPINI1 TRNL1 WWOX SCN8A NDUFS8 MECP2 GABRB2 GUF1 KCNA2 ST3GAL3 NDUFS6 SH2D1A TRNC SLC12A3 MAPK10 GLUL SPTAN1 D2HGDH ARHGEF9 SUCLA2 GABRA5 PPP3CA NDUFS3 NDUFB9 ZNHIT3 NDUFB3 CPLX1 STAT2 GABRB1 SLC6A9 KCNQ2 HADH LIAS GABRB2 KYNU PIGA TCF4 PNPT1 TIMMDC1 NUS1 KCNA2 AMT SZT2 FGF12 HNRNPU TBCE NECAP1 HIBCH TUFM FOXRED1 EEF1A2 CUX2 ND3 CNPY3 ACTL6B CNKSR2 ACSF3 DGUOK UNC80 TBCE NTRK2 NRXN1 TMEM126B ND5 TH CNTNAP2 SYNJ1 NDUFAF1 PCCA PNPO KCNB1 ATP6V1A SYNGAP1 AMACR CLCNKB NDUFAF2 SIK1 FRRS1L TP53 PMPCB CLTC DNM1 SLC1A2 DPM2 GLDC HTRA1 TBCD GABRA1 NDUFS4 RNASEH2B GCDH SLC35A2 ETHE1 SCN2A CHD2 SYNJ1 DLD
Protein Mutations 1
A3243G
SNP 0