Mode
Text Size
Log in / Sign up
Phase 3 N=105 Randomized Treatment

KIDCARE (Kawasaki Disease Comparative Effectiveness Trial)

Mucocutaneous Lymph Node Syndrome

Enrolled (actual)
105
Serious AEs
35.9%
Results posted
Dec 2021
Primary outcome: Primary: Number of Participants With Cessation of Fever Within 24h of Initiation of Study Treatment With no Fever Recurrence Within Next 7 Days. — 25; 40 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
IVIG (Drug); Infliximab (Drug)
Age
Pediatric
Sex
All
Sponsor
University of California, San Diego
Primary completion
Aug 2020

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Cessation of Fever Within 24h of Initiation of Study Treatment With no Fever Recurrence Within Next 7 Days.
25; 40
SECONDARY
Change in White Blood Cell Count (WBC) Between Baseline and 24 Hours and 2 Weeks Following Study Treatment.
-2.05; 0.15; -4.9; -3.5
SECONDARY
Change in Zworst Score Between Baseline and 2-week (± 4 Days) Echocardiograms
-0.31; -0.01
SECONDARY
Total Number of Fever Days (24 Hour Period With a T≥38.0°C) From Enrollment
2; 1
SECONDARY
Duration of Hospitalization
4; 2.5
SECONDARY
Number of Participants With IVIG and Infliximab Infusion Reactions and Complications
1; 2
SECONDARY
Change in Absolute Neutrophil Count (ANC) Between Baseline and 24 Hours and 2 Weeks Following Study Treatment.
-3398.4; -1742; -5853.5; -4661.0
SECONDARY
Change in C-reactive Protein (CRP, mg/dL) Concentration Between Baseline and 24 Hours and 2 Weeks Following Study Treatment.
-4.6; -4.7; -8.6; -13.4

Summary

Kawasaki disease (KD) is a self-limited illness that affects the heart blood vessels (coronary arteries) of infants and children and is now the most common cause of acquired heart disease in children. A mixture of proteins from human blood (Intravenous immunoglobulin, IVIG) is a treatment that reduces the rate of the major complication of the disease: a bulging of the wall of the coronary arteries called an aneurysm. However, 10-20% of children are resistant to this treatment and the fever returns. These children have the highest rates of aneurysm formation and thus should be treated aggressively. Unfortunately, there are no guidelines for the best secondary treatment for these resistant patients because the problem has never been adequately studied. Most physicians choose either a second infusion of IVIG or an engineered antibody called infliximab that inactivates a molecule that promotes inflammation. This trial will randomize (assign by chance like the flip of a coin) IVIG-resistant patients to receive either a second IVIG infusion or infliximab and the response to treatment will be compared to learn which treatment stops the fever the fastest. In addition, parents and caregivers will provide observations about their child's response to the different treatments.

Eligibility Criteria

Inclusion Criteria

  • Eligible subjects will be as follows:
  • 4 weeks to 17 years of age,
  • fulfill the American Heart Association case definition for complete or incomplete KD,
  • have had fever (T ≥38°C) for 3 to 10 days prior to initial IVIG treatment,
  • have fever (T ≥38°C orally or rectally) between 36 hours and 7 days after end of the first IVIG infusion without other likely cause

Exclusion Criteria

  • Patient treated with infliximab or steroids for present illness (pts who received oral steroids as outpatients prior to KD diagnosis but who otherwise qualify for the study will not be excluded)
  • Known prior infection with tuberculosis, coccidiomycosis, or histoplasmosis.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03065244). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search