Status:

COMPLETED

Efficacy of Vaccination Against COVID-19 in Patients Presenting a Neuromuscular Disease With Severe Amyotrophy

Lead Sponsor:

University Hospital, Bordeaux

Conditions:

Neuromuscular Diseases

COVID-19

Eligibility:

All Genders

18+ years

Brief Summary

Des vaccins sont désormais disponibles en France, dont le vaccin Moderna COVID-19 qui est basé sur la technologie des ARNm. La séquence génétique qu'il contient code pour la protéine Spike (S) de l'en...

Detailed Description

COVID-19 is linked to SARS-CoV-2, a new coronavirus that can lead to death. Some neuromuscular patientsare considered at risk for various reasons: cardiomyopathy or rhythm and/or conduction disorder, ...

Eligibility Criteria

Inclusion

  • Inclusion Criteria
  • \- For patients with severe neuromuscular disease:
  • Adult over 18
  • Person with a defined severe neuromuscular pathology by a modified Rankin score ≥ 4
  • Person supported at the YDK pole
  • Person who has received vaccination with the Moderna vaccine, in the quadriceps or deltoid
  • Non-objection of the patient and/or his legal representative to the participation in the study
  • For patients in the negative control group :
  • Non-objection of the patient to the storage and use in the framework of the CANNEMUSS study of these blood samples from the routine care.
  • Patient having had a blood sample taken as part of the treatment for virological analysis before anti-COVID 19 vaccination.
  • Patient matched in sex and age to a patient included in the study CANNEMUSS.
  • For patients in the positive control group :
  • Non-objection of the patient to the storage and use in the framework of the CANNEMUSS study of these blood samples from the routine care.
  • Patient having had a blood sample taken as part of the treatment for virological analysis following infection with the omicron variant.
  • Exclusion Criteria for patients with neuromuscular disease severe
  • Person with symptomatic infection with SARS-CoV-2 proven by a positive PCR
  • Person with Amyotrophic Lateral Sclerosis

Exclusion

    Key Trial Info

    Start Date :

    September 1 2021

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ACTUAL

    End Date :

    September 1 2022

    Estimated Enrollment :

    36 Patients enrolled

    Trial Details

    Trial ID

    NCT05353738

    Start Date

    September 1 2021

    End Date

    September 1 2022

    Last Update

    October 6 2023

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    University Hospital of Bordeaux

    Bordeaux, France, 33 000