Last updated: February 20, 2023
Sponsor: Hippocration General Hospital
Overall Status: Active - Not Recruiting
Phase
3
Condition
Chest Pain
Cardiovascular Disease
Heart Disease
Treatment
N/AClinical Study ID
NCT05737680
RESTORE
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Male or female patients aged≥18 years
- Idiopathic recurrent pericarditis with at least 2 recurrences
- Recurrent pericarditis defined as a first episode of acute pericarditis followed byrecurrences (at least two recurrences for this study). First episode of pericarditisis diagnosed when at least two of the following criteria were present: pericarditistypical chest pain (sharp and pleuritic, improved by sitting up and leaning forward),pericardial friction rubs, widespread ST segment elevation or PR interval (PR)depressions not previously reported, and new or worsening pericardial effusion.Recurrence is diagnosed when chest pain recurs and one or more of the following signsis present: fever, pericardial friction rub, ECG changes, echocardiographic evidenceof new or worsening pericardial effusion, and elevations in the white blood cellcount, erythrocyte sedimentation rate or C-reactive protein. To be enrolled in thisstudy, elevation of C-reactive protein is mandatory both in the first attack and inthe following recurrences. The investigators differentiate recurrences from incessantpericarditis, term used to define patients with continued activity of pericarditis (with a symptom-free interval of < 6 weeks)
- Specific aetiologies excluded, including tuberculous, neoplastic or purulentaetiologies, post-cardiac injury syndromes, and rheumatic autoimmune diseases.
- Female subjects must be postmenopausal, or incapable of pregnancy or permanentlysterile, or if of childbearing potential must agree to use highly-effective method ofcontraception.
- Signed written informed consent by the patient for participation in the study andagreement to comply with the medication and the follow-up schedule.
Exclusion
Exclusion Criteria:
- Ophthalmologic contraindications
- Structural heart disease
- Corrected QT interval >440msec in men and >450msec in women
- Left ventricular hypertrophy >13mm in men and >11mm in woman
- Known allergy or intolerance to hydroxychloroquine
- Life expectancy of < 12 months
- Complex congenital heart disease
- History of ventricular arrhythmias other than isolated extrasystoles
- Women who are pregnant (as evidenced by pregnancy test if pre-menopausal)
- Known channelopathy such as Brugada syndrome, long QT syndrome, or Catecholaminergicmonomorphic ventricular tachycardia
- On the heart transplant list
Study Design
Total Participants: 30
Study Start date:
February 01, 2023
Estimated Completion Date:
December 31, 2024
Study Description
Connect with a study center
"Hippokration" General Hospital of Athens
Athens, Attiki 11527
GreeceSite Not Available
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