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Clinical Trials/NCT04922905
NCT04922905
Completed
Not Applicable

Nervous System Symptoms Associated With COVID 19 : NS-COV

University Hospital, Toulouse1 site in 1 country99 target enrollmentApril 2, 2020
ConditionsCovid19

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Covid19
Sponsor
University Hospital, Toulouse
Enrollment
99
Locations
1
Primary Endpoint
percentage of patients in the Neuro + and Neuro- groups
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

This study aim to prospectively evaluate the neuropsychiatric symptoms of patients infected with the SARS-CoV-2 virus by a standardized neuropsychiatric examination : the global CASE scale (Clinical Assessment Scale in Autoimmune Encephalitis), and the prevalence of disturbances of consciousness, focal neurological deficit, cognitive impairment, headache, anosmia, sleep disturbances, impaired autonomic nervous system and peritraumatic stress.

Registry
clinicaltrials.gov
Start Date
April 2, 2020
End Date
April 2, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Being hospitalized at the Toulouse University Hospital for a COVID-19 infection proven by a probable PCR or COVID-type examination on the chest scan
  • Have given oral consent for the collection of clinical neurological data
  • Be in a clinical state compatible with a 30-minute neurological examination
  • Be French-speaking
  • Be affiliated to a Social Security scheme

Exclusion Criteria

  • Refusal of the neurological examination
  • History of neurological pathology at a severe stage
  • Pregnant or breastfeeding woman
  • Persons with tutors or curators

Outcomes

Primary Outcomes

percentage of patients in the Neuro + and Neuro- groups

Time Frame: Baseline T0 : inclusion visit

The percentage is deducted from the score on a global scale by the Clinical Assessment Scale in Autoimmune Between 0 and 1, patients will be classified in the Neuro group, if this score is greater than or equal to 2, patients will be classified in the Neuro + group.

Study Sites (1)

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