Last updated: April 6, 2023
Sponsor: Istituto Giannina Gaslini
Overall Status: Active - Not Recruiting
Phase
3
Condition
Chest Pain
Cardiovascular Disease
Cardiac Disease
Treatment
N/AClinical Study ID
NCT05805930
CREATE
Ages 8-18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Male and female patients.
- Parent or legal guardian written informed consent and child assent, if appropriate,are required before any assessment is performed.
- Diagnosis of relapse of pericarditis in a patient with previous diagnosis of acutepericarditis (idiopathic or secondary to invasive cardiac procedures).
- Inadequate response or intolerance to non-steroidal anti-inflammatory drugs orcolchicine
Exclusion
Exclusion Criteria: 1. Pericarditis secondary to a known infection (viral, bacterial, mycobacterial). 2. Pericarditis in a patient with a previous diagnosis of any neoplasm and withoutcomplete recovery from at least one year. 3. Pericarditis in the context of a systemic disease. 1. Patients fulfilling diagnostic criteria for an autoimmune systemic disease 2. Patients with a previous diagnosis of a genetically confirmed autoinflammatorydisease 4. Any conditions or significant medical problems, which in the opinion of theinvestigator places the patient at unacceptable risk for immunomodulatory therapy. 5. Main alteration in the blood count 6. Presence of Human Immunodeficiency Virus (HIV) infection, Hepatitis B or Hepatitis Cinfections. 7. Evidence of active or latent tuberculosis (TB) determined by positive QuantiFERON (QFT-TB G In-Tube) test or positive Purified Protein Derivative (PPD) test (≥5 mminduration) within 2 months prior to randomization. 8. Administration of any investigational drug or implantation of investigational device,or participation in another trial, within 30 days before screening. 9. Use of steroids at the dosage of 1 mg/kg/day of prednisone or equivalent for at least 5 days in the 30 days before randomization. 10. Live vaccinations within 1 months prior to the start of the trial and during thetrial. 11. Pregnancy, confirmed by a positive hCG laboratory test. 12. Female adolescents (≤18 years of age) of childbearing potential who do not agree toabstinence or, if sexually active, do not agree to the use of contraception.
Study Design
Total Participants: 48
Study Start date:
June 01, 2023
Estimated Completion Date:
May 31, 2026