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Neurological manifestations of COVID-19

NEPSycon-COVID: Assessment of Neurological, Epidemiological, Psychiatric and Psychosocial Consequences during the COVID -19 Pandemicâ?? - NEPSycon-COVID

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2020/08/027490
Enrollment
200
Registered
2020-08-31
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: G998- Other specified disorders of nervous system in diseases classified elsewhere Health Condition 2: B338- Other specified viral diseases

Interventions

None listed

Sponsors

NIHRLiverppol University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Methodology: Participants: All neurological patients visiting the neurological emergency with the following inclusion and exclusion criteria will be included into the study: 1. Inclusion criteria: a. Patients of Neurological disorders with previously described symptoms related to COVID-19 infection such as: Young Stroke (cerebrovascular accident), Stroke (cerebrovascular accident) patients with deranged prothrombotic states/elevated D-dimer assays, Acute encephalitis, Seizure of unknown etiology, Guillain barre syndrome, Myositis with elevated CPK, para-infectious neurological disorders in the form of myelitis, ADEM, CNS Demyelinating disorders b. Patients of neurological disorders precipitated or preceded by respiratory symptoms in the last 2-4 weeks c. Patients of neurological symptoms (not fitting the criteria of a/b) but found to have lymphopenia / thrombocytopenia /thrombotic states / elevated D-dimer levels 2. Exclusion criteria: a. Patients of neurological disorders with a known etiology other than COVID-19 b. Not giving consent for the study Patients of neurological disorders with suspected COVID-positivity will be included into the study after fulfilling the inclusion and exclusion criteria. Then, they will undergo following assessment for further characterization of the neurological symptoms and signs.

Exclusion criteria

Exclusion criteria: 2. Exclusion criteria: a. Patients of neurological disorders with a known etiology other than COVID-19 b. Not giving consent for the study

Design outcomes

Primary

MeasureTime frame
The primary outcome will be death. Secondary outcomes of interest will be proportions of patients with each neurological diagnosis in the group with neurological disease; admission to a critical (intensive/high dependency) care unit; time to discharge from hospital; and functional outcome at discharge (or 30 days from admission, if still in hospital) - Timepoint: At initial diagnosis and then at 1 month, 3 months, 6 months and 12 months

Secondary

MeasureTime frame
Drugs on and during admission, such as anticoagulants and antiplatelets 1.SARS-CoV-2 viral load on upper respiratory tract specimen 2.Gender 3.Ethnicity 4.Comorbidities: diabetes, hypertension, obesity, HIV and other immunosuppression 5.Serum C-reactive protein 6.Blood D-dimer concentration 7.Pre-admission general health state (using Clinical Frailty Scale). Timepoint: At initial diagnosis and then at 1 month, 3 months, 6 months and 12 months

Countries

India

Contacts

Public ContactRavi Vasanthapuram

National Institute of mental health & Neurosciences (NIMHANS), Bangalore 29

sundernetra@yahoo.co.in9880106662

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026