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 (11)


Name (Synonyms) Correlation
drug453 EP Wiki 0.58
drug324 Clevudine Wiki 0.58
drug275 CT-scan Wiki 0.58
drug451 EEG Wiki 0.58
drug319 Ciclesonide Metered Dose Inhaler [Alvesco] Wiki 0.58
drug316 Ciclesonide Wiki 0.58
drug1094 Pulse oximetry Wiki 0.58
drug213 Blood tests Wiki 0.41
drug525 Follow up Wiki 0.41
drug591 Hydroxychloroquine Wiki 0.12
drug1016 Placebo Wiki 0.04

Correlated MeSH Terms (3)


Name (Synonyms) Correlation
D020196 Trauma, Nervous System NIH 0.58
D003693 Delirium NIH 0.41
D016638 Critical Illness NIH 0.23

Correlated HPO Terms (1)


Name (Synonyms) Correlation
HP:0001298 Encephalopathy HPO 0.82

There are 3 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, phone call, 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

Description: A favorable outcome is defined by a Glasgow Outcome Scale Extended (GOSe) >= 5. The Glasgow Outcome Scale Extended (GOSe) will be determined patients charts review, phone call, and/or general practitioner interview conducted by an independent assessor. The GOSe score : [1: Death, 2: Persistent vegetative state, 3: Severe disability Lower, 4: Severe disability Upper, 5: Moderate disability Lower, 6: Moderate disability Upper, 7 : Good recovery lower, 8 : Good recovery Upper]

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

3 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


HPO Nodes


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