Last updated: May 6, 2024
Sponsor: University of Virginia
Overall Status: Active - Recruiting
Phase
4
Condition
Congestive Heart Failure
Chest Pain
Heart Failure
Treatment
Control/Placebo group
Colchicine 0.6 mg
Clinical Study ID
NCT06286423
HSR220446
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Primary admission diagnosis of acute decompensated heart failure as evidenced by:
- Heart failure symptoms and at least one of the following:
- Pulmonary congestion/edema at physical exam (or chest radiography)
- E/e' > 13 on transthoracic echocardiography
- Left heart catheterization showing elevated left ventricular (LV) end-diastolicpressure >18 mmHg or right heart catheterization showing pulmonary arteryoccluding pressure (wedge) >16 mmHg
- Elevated plasma B-type natriuretic peptide (>100 pg/ml) or N-terminal B-typenatriuretic peptide (>300 pg/ml)
- LV systolic dysfunction (left ventricular ejection fraction [LVEF] <40%) during theindex hospitalization or prior 12 months;
- Expected duration of heart failure at least three months
- Age 18 years or older
- Willing and able to provide written informed consent
- Screening plasma CRP >0.3 mg/dL (3 mg/L) or high-sensitivity CRP >2 mg/L
Exclusion
Exclusion Criteria:
- Concomitant clinically significant comorbidities that would interfere with theexecution or interpretation of the study, including but not limited to acute coronarysyndromes, uncontrolled hypertension or orthostatic hypotension, tachy- orbrady-arrhythmias, acute or chronic pulmonary disease or neuromuscular disordersaffecting respiration
- Cardiac resynchronization therapy (CRT), coronary artery revascularization procedures,or heart valve surgeries performed within 3 months or planned during the admission
- Previous or planned implantation of left ventricular assist devices or hearttransplantation
- Chronic use of intravenous inotropes
- Current or recent (i.e. within 4 half-lives) use of immunosuppressive oranti-inflammatory drugs (not including NSAIDs).
- Current treatment with colchicine or planned initiation of colchicine therapy in thenext three months for gout
- Chronic inflammatory disorder, including but not limited to rheumatoid arthritis andsystemic lupus erythematosus
- Active infection (of any type)
- Chronic or recurrent infectious disease, including hepatitis B virus, hepatitis Cvirus, and HIV/AIDS
- Prior (within the past 5 years) or current malignancy, with the exclusion of in situlesion with low potential for progression
- Any comorbidity leading to expected survival less than three months or inability tocomplete the study
- End-stage kidney disease requiring renal replacement therapy
- Neutropenia (<2,000/mm3) or Thrombocytopenia (<50,000/mm3)
- Pregnancy
- For all biological females with child bearing potential a pregnancy test will beperformed as part of standard of care.
- Presence of specific contraindications to colchicine treatment, which may include
- Previous adverse reaction to colchicine
- Biliary obstruction
- Renal impairment with estimated glomerular filtration rate (eGFR) <30 ml/min
- Liver cirrhosis from stage Child-Pugh A to more advanced
- Prisoners
- Treatment with medication contraindicated for concomitant use with colchicine per Food and Drugs Administration labeling, including:
- Protease inhibitors
- Macrolides antibiotic
- Ketoconazole, Fluconazole and Itraconazole
- Nefazodone
- Non-dihydropiridine calcium channel blockers
- Aprepitant
- Ranolazine
- Cyclosporine
Study Design
Total Participants: 30
Treatment Group(s): 2
Primary Treatment: Control/Placebo group
Phase: 4
Study Start date:
June 01, 2024
Estimated Completion Date:
June 30, 2028
Study Description
Connect with a study center
UVA Health
Charlottesville, Virginia 22908
United StatesActive - Recruiting
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