AzTrials
AzTrials

Kawasaki DiseaseNCT04538495

Characterization of Multisystem Inflammatory Syndrome in Children (MIS-C) and Its Relationship to Kawasaki Disease

An observational study of Kawasaki Disease and Inflammation, run by University of California, San Diego at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

Beginning in mid-March 2020, pediatricians in communities in Western Europe, the UK, and the Eastern U.S. that had been severely affected by the Covid-19 pandemic noted an increased number of children presenting with fever and evidence of severe inflammation who required admission to intensive care. Read more about this study

Who is it for?
Ages 1 month and older
Conditions the study is for
Kawasaki Disease, Inflammation
How many people
268 participants
Where
1 siteUnited States
Study dates
1 Aug 2020to 31 Mar 2022
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 1 month and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: We plan to enroll 100 MIS-C subjects in this study to allow for the collection of data and samples that will support the many different aims in this study.

Who may be able to join

  • The following patients (age 1 mos. through young adults) will be recruited for this study:
  • Patients who meet the CDC definition for MIS-C:
  • Patients presenting with fever (>38C for >24 h - also by subjective report), laboratory evidence of inflammation, and evidence of clinically severe illness requiring hospitalization, with multisystem (>2) organ involvement (cardiac, renal, respiratory, hematologic, gastrointestinal, dermatologic or neurological); AND
  • No alternative plausible diagnoses; AND Positive for current or recent SARS-CoV-2 infection by RT-PCR, serology, or antigen test; or suspected COVID-19 exposure within the 4 weeks prior to the onset of symptoms
  • Patients who meet the CDC definition for MIS-C and require care in the PICU

Who cannot join

  • All patients with pre-existing major medical conditions will be excluded. This includes patients with known genetic disorders (e.g. trisomy 21, cystic fibrosis), conditions requiring continuous medication (e.g. seizure disorder, heart disease), or known immune disorder (e.g. hypogammaglobulinemia, complement deficiency). Patients with asthma or atopic dermatitis will not be excluded unless patients have received oral steroids in the previous week. Obesity is not an exclusion.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • University of California, San Diego

    La Jolla, California, 92093

Other trials in United States

About this study

Beginning in mid-March 2020, pediatricians in communities in Western Europe, the UK, and the Eastern U.S. that had been severely affected by the Covid-19 pandemic noted an increased number of children presenting with fever and evidence of severe inflammation who required admission to intensive care. The syndrome was branded by the CDC in the U.S. as Multisystem Inflammatory Syndrome in Children (MIS-C). The most severely affected children presented with heart failure leading to shock and the absence of significant pulmonary disease. The clinical presentation in these patients shared many features with Kawasaki disease (KD), a self-limited pediatric vasculitis that can result in coronary artery aneurysms.The inflammatory markers, however, were much higher even than KD shock syndrome, a variant of KD presenting with distributive shock and requiring inotropic and vasoactive support in the ICU. Some patients were polymerase chain reaction (PCR)+ for SARS-CoV-2 while most were virus-negative but had detectable antibody suggesting that MIS-C was an immune-mediated reaction to antecedent exposure to the virus. While patients were being diagnosed with shock and MIS-C, children with a milder version of MIS-C that shared many features of KD were being diagnosed in these same regions.

Read the detailed description

Clinical characterization (Burns, Tremoulet, Sivilay, Roberts, Jain): Over the 8 months of enrollment funded by this supplement, 30 sites will collect data on KD and MIS-C patients using the detailed case report form in our REDCap database. This includes data on patient demographics, clinical presentation, laboratory data, treatments, clinical outcomes, and cardiovascular outcomes on all KD and MIS-C patients so that the investigators can develop a systematic picture of the different patient groups (see details below).

Parent observations (Kim): To learn about signs and symptoms in the patient and family members leading up to acute presentation a parent questionnaire will be devised and analyzed by Dr. Katherine Kim with the Patient and Parent Advisory Board. The investigators will collect known signs and symptoms as well as those that may not have been previously reported in the literature and record presence/absence, location in the body, and severity level by day. The questionnaire will be available as a mobile/web application and via paper. With these data, the investigators will conduct an exploratory analysis to characterize symptom phenotypes and the relationships of these profiles with demographic features and clinical characteristics. In addition, the investigators will assess whether we can detect differences between the symptom phenotypes of KD and MIS-C. The investigators will conduct cluster analysis to identify symptom phenotypes from aggregate symptom observations blinded as to presumed or verified diagnosis (n=100 with each sign/symptom on each day as a distinct data point). Phenotypes may include characteristics such as symptoms that co-occur or are independent, and symptom burden index (e.g., number symptoms present). The investigators will use Ward's hierarchical cluster analysis to estimate the number of likely clusters.3 The investigators will apply K-means nonhierarchical cluster analysis repeated 100 times in a leave-one out validation model to assure repeatability and stability within the model. The investigators will create score indices analyzed with logistic regression, principal component analysis, factor analysis and correlation analysis. The investigators will then assess whether clusters are related to verified diagnosis and/or sociodemographic characteristics such as age, race/ethnicity, geography. The investigators will use discriminant analysis techniques and more recent classification techniques such as CART to examine if symptom phenotypes of KD and MIS-C are dissimilar. If information in terms of symptom clusters at a point in time or a trajectory of a single symptom over time are insufficient to distinguish between the two conditions, this would provide support for the argument that the recorded symptoms are insufficient for discrimination or that the two disease entities are not symptomatically different. This exploratory analysis will provide important information that can be further developed for clinical guidance and parent education.

Photography (Kim, Tremoulet): Patient photographs of the eye, mouth/tongue, and rash will be collected as a novel addition to the usual clinical data. These photographs obtained before treatment will document the presence or absence of conjunctival injection and perilimbal sparing, mucocutaneous changes in the oropharynx including changes in the vermillion border (erythema, fissuring) and the tongue (strawberry tongue), and the nature of the rash. The photographs will be subjected to analysis using facial recognition software and artificial intelligence approaches used by our collaborators at the University of Southern California Center for Artificial Intelligence in Society led by Hayden Shively and Lucas Hu to evaluate whether a computer algorithm can be created that can differentiate the clinical characteristics of MIS-C from photographs taken of children with acute KD and those with other pediatric febrile illnesses. Dr. Katherine Kim at UC Davis will compare the photos with the questionnaire responses to supplement the parent descriptions of signs and symptoms and validate the observations. This comparison can result in enhanced descriptions using the words of parents themselves. Photography is needed to document these physical findings as the investigators have learned over the years that physician description of these features is woefully inaccurate. The finding, for example, of a strawberry tongue is a specific injury pattern that involves sloughing of the cornified tips of the filiform papillae and has historically been associated with only 3 conditions: staphylococcal and streptococcal toxin-mediated disease and KD.

Medical subject headings
Mucocutaneous Lymph Node Syndrome, Inflammation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Collection of clinical data and patient samples from children with MIS-C and KD to

    Collection of clinical data and patient samples from children with MIS-C and KD to understand the relationship between these two conditions.

    Measured: We will collect demographic and clinical data on all KD patients at participating sites throughout the 8-month study period.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Sep 2020
  2. Study start1 Aug 2020
  3. Primary completion1 Aug 2021
  4. Study completion31 Mar 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Prospective
Enrolment
268 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04538495
Sponsor's protocol ID
CER-1602-34473
Status last verified
Nov 2021
First submitted
19 Aug 2020
Last updated
1 Aug 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Kawasaki Disease and Inflammation, run by University of California, San Diego at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 1 Aug 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Collection of clinical data and patient samples from children with MIS-C and KD to (time frame: We will collect demographic and clinical data on all KD patients at participating sites throughout the 8-month study period.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Aug 2025.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in