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Study of Virus-specific Lymphocytic Cell Populations in Non-invasive Nasal Mucosa Samples of MIS-C Patients

M

Medical University of Warsaw

Status

Enrolling

Conditions

COVID-19
MIS-C Associated With COVID-19

Study type

Observational

Funder types

Other

Identifiers

NCT05560906
NAWA015

Details and patient eligibility

About

The aim of the study is to make an accurate assessment of immune cells obtained from nasal mucosa and peripherial blood of MIS-C patients during the disease and the period of health.

Full description

The study will consist of two parts. Initially, it will be of a cross-cutting comparative nature, when a group of healthy patients (control group) and a group of patients diagnosed with MIS-C/PIMS syndrome are compared with each other, based on nasal curettage swabs and peripheral blood, before the inclusion of systemic anti-inflammatory treatment (study group). In addition, an observation of the research group will be carried out, during which swabs and peripheral blood will be taken at two more control points.

Enrollment

20 estimated patients

Sex

All

Ages

Under 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • MIS-C diagnosis based of WHO diagnostic criteria.

Exclusion criteria

  • immunosuppressive treatment received up to 3 months before
  • intranasal drugs received up to 7 days before
  • COVID-19 vaccination
  • no consent

Trial design

20 participants in 2 patient groups

Control group
Description:
Healthy patients under 18 years of age.
MIS-C group
Description:
Patients with MIS-C diagnosed, based on WHO diagnostic criteria.

Trial contacts and locations

1

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Central trial contact

Ziemowit Strzelczyk; Wojciech Feleszko, MD., PhD

Data sourced from clinicaltrials.gov

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