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Evaluation of Biological Response to SARS-COV2 (COVID-19) in Patients With Pre-existing Neurological Disease or Newly Neurological Symptoms (BIO-COCO-NEUROSCIENCES)

A

Assistance Publique - Hôpitaux de Paris

Status

Completed

Conditions

Neurologic Manifestations
Psychiatric Manifestations
Covid19

Treatments

Other: blood sample

Study type

Interventional

Funder types

Other

Identifiers

NCT04568707
APHP200845

Details and patient eligibility

About

Patients with neurological or psychiatric symptoms or pre-existing disease will be sampled (blood for serum and DNA or saliva for DNA) at inclusion and at M6 (blood) and M12 (blood) depending on their pathology. Sampling will be done either at hospital if patient is on site for routine care or at home if no consultation is scheduled at hospital.

Enrollment

238 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

  1. Age over 18 yo

  2. Patient having presented or presenting a Covid-19 infection defined by a positive PCR or a typical chest scanner of Covid-19 infection or a positive serology or a typical clinical picture in a pandemic period

  3. And patient with:

    1. a neurological or psychiatric manifestation de novo during or after the Covid-19 infection and/or
    2. either a chronic neurological or psychiatric pathology

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

238 participants in 1 patient group

Covid-19 infection
Experimental group
Description:
Covid-19 infection defined by a positive PCR or a typical chest scanner of Covid-19 infection or a positive serology or a typical clinical picture in a pandemic period
Treatment:
Other: blood sample

Trial contacts and locations

1

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Central trial contact

Céline LOUAPRE, MD; Jean-Christophe CORVOL, MD,PHD

Data sourced from clinicaltrials.gov

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