MOIS-CoR: MultiOrgan Inflammatory Syndromes COVID-19 Related Study

Sponsor
Medical University of Warsaw (Other)
Overall Status
Recruiting
CT.gov ID
NCT04811456
Collaborator
Wrocław Medical University (Other), University of Warsaw (Other)
1,000
2
63
500
7.9

Study Details

Study Description

Brief Summary

The study comprise a nationwide, voluntary, on-line survey of inflammatory syndromes in children for retrospective (since 4th March 2020) and prospective data collection. Our aim was to capture and describe multisystem inflammatory syndrome in children (MIS-C) in Poland.

Condition or Disease Intervention/Treatment Phase
  • Other: multisystem inflammatory syndrome in children (MIS-C)

Detailed Description

The voluntary surveillance for retrospective (since 4th March) and prospective data collection was initiated under the National Consultant of Pediatrics auspices. Anonymized patient data from pediatric hospitals from all over the country are extracted from electronic and paper records and collected through online form developed for that purpose. Before the surveillance was launched, reporting clinicians underwent an online training, which included the current state of knowledge about multisystem inflammatory syndrome in children (MIS-C). Patient management is at the discretion of the relevant treating clinicians.

KD and aKD were defined following the American Heart Association (AHA) guidelines.

TSS was established based on modified criteria by the Centers for Disease Control and Prevention.

MAS was diagnosed based on the Paediatric Rheumatology International Trials Organization (PRINTO) criteria for MAS classification.

The definition of the inflammatory syndrome was based on the WHO MIS-C definition with the exclusion of SARS-CoV-2 confirmation.

For patients who met the inclusion criteria, demographic data, past medical history, data on COVID-19 exposure, clinical symptoms, physical examination findings, laboratory, imaging, and cardiologic tests results, treatment, and outcome data are collected.

All study definitions are defined in accordance to relevant guidelines and evaluated automatically with the use of a dedicated software.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
1000 participants
Observational Model:
Case-Only
Time Perspective:
Cross-Sectional
Official Title:
MultiOrgan Inflammatory Syndromes COVID-19 Related Study
Actual Study Start Date :
May 25, 2020
Anticipated Primary Completion Date :
May 25, 2025
Anticipated Study Completion Date :
Aug 25, 2025

Arms and Interventions

Arm Intervention/Treatment
MIS-C

Cases fulfilling following criteria: fever ≥3 days at least two of the following: rash or bilateral conjunctivitis or mucocutaneous inflammation signs hypotension features of myocardial dysfunction, pericarditis, or coronary artery abnormality, based on echocardiographic findings or elevated B-type natriuretic peptide (BNP)/N-terminal-pro-BNP (NT-proBNP) or troponin evidence of coagulopathy acute gastrointestinal problems elevated inflammatory markers AND no other apparent microbial cause evidence of COVID-19 (positive real-time polymerase chain reaction, antigen test or serology), or personal history of COVID-19 or contact with a proven COVID-19 case

Other: multisystem inflammatory syndrome in children (MIS-C)
as in group description

Outcome Measures

Primary Outcome Measures

  1. PICU [5 years]

    pediatric intensive care unit treatment need

Secondary Outcome Measures

  1. Heart dysfunction [5 years]

    Heart dysfunction is defined as ejection fraction (EF) of <55% and severe heart dysfunction as EF <35%.

  2. CAA [5 years]

    Coronary artery abnormalities comprise both coronary dilation and/or coronary aneurysm. Dilation was defined by Z-score between 2 to 2.5, while aneurysm by Z score ≥2.5

  3. Hypotension [5 years]

    Hypotension is defined by a minimal systolic blood pressure (sBP) below 70+2×age (in years) mmHg or below 90 mmHg for children >10 years old

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • patients who required hospitalization since 4th March 2020;

  • diagnosed Kawasaki disease (KD) or incomplete (atypical) Kawasaki disease (aKD) or toxic shock syndrome (TSS) or macrophage activation syndrome (MAS) or unspecified inflammatory syndrome;

Exclusion Criteria:
  • other infectious and non-infectious causes that could be responsible for the disease

SARS-CoV-2 polymerase chain reaction (PCR) or serology result could have been positive or negative. Due to limited availability and reliability of serologic testing, proven or likely COVID-19 criterion was not a condition determining inclusion to the registry.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Medical University of Warsaw Children's Hospital Warsaw Poland 02091
2 Wroclaw Medical University Wrocław Poland 50-368

Sponsors and Collaborators

  • Medical University of Warsaw
  • Wrocław Medical University
  • University of Warsaw

Investigators

  • Principal Investigator: Magdalena Okarska-Napierała, Medical University of Warsaw

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Medical University of Warsaw
ClinicalTrials.gov Identifier:
NCT04811456
Other Study ID Numbers:
  • MOIS-CoR
First Posted:
Mar 23, 2021
Last Update Posted:
Mar 26, 2021
Last Verified:
Mar 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Medical University of Warsaw
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 26, 2021