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Prospective Registry of Corona Virus Disease 2019 (Covid-19) Patients With Neuromuscular Involvement

U

University Hospital Tuebingen

Status

Unknown

Conditions

Sars-CoV2
Myositis
Corona Virus Infection
Myocarditis
COVID

Treatments

Diagnostic Test: muscle ultrasound
Diagnostic Test: laboratory biomarkers

Study type

Observational

Funder types

Other

Identifiers

NCT04367350
246/2020BO2

Details and patient eligibility

About

Prospective registry for multimodal assessment of neuromuscular pathology associated with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, enrolling consecutive patients with corona virus disease 2019 (Covid-19), who are admitted to the intensive care unit of the department of anesthesiology and intensive care medicine, or the department of neurology at Tübingen University Hospital.

Full description

The prospective registry shall provide new insights into muscular involvement associated with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. For that reason consecutive patients with proven corona virus disease 2019 (Covid-19), who are admitted to the intensive care unit of the department of anesthesiology and intensive care medicine, or the department of neurology at Tübingen University Hospital, are enrolled. Multimodal assessment of neuromuscular pathology is based on medical history, laboratory biomarkers including inflammation parameters and autoimmune antibodies, vital parameters monitoring, muscle ultrasound, transthoracic echocardiography, electroneurography, as well as electromyography. Inclusion of follow-up visits permit longitudinal and prognostic evaluation of diagnostic and therapeutic interventions (e.g. immunomodulation with immunoglobulins, corticosteroids, or interleukin 6 receptor antagonists).

Enrollment

500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥ 18 years
  • Proven severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection

Exclusion criteria

  • active or known history of myopathy or advanced stage neuropathy
  • refusal to participate in clinical research

Trial contacts and locations

1

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Central trial contact

Alexander Grimm, MD; Sven Poli, MD

Data sourced from clinicaltrials.gov

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