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Colchicine and Inflammation in Aortic Stenosis (CHIANTI)

R

Radboud University Medical Center

Status and phase

Active, not recruiting
Phase 3

Conditions

Calcification
Inflammation
Aortic Valve Stenosis
Aortic Valve Disease
Cardiovascular Diseases
Aortic Valve Calcification

Treatments

Drug: Colchicine
Drug: Placebo

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Aortic stenosis (AS) is the most common valvular heart disease in the developed world. Once symptomatic, untreated patients have a poor prognosis with five-year survival rate of 25%. Once at an advanced stage, AS will lead to the development of left ventricle hypertrophy, and eventually heart failure and death. At-present, there is no effective medical therapy for aortic stenosis. Current management of patients with AS consists of 'watchful waiting'. Valve replacement is needed when these patients (often acutely) become symptomatic. Recent studies have shown that inflammatory processes with similarities to atherosclerosis play an important role in AS. Therefore, we hypothesize that treatment with anti-inflammatory therapy, in the form of colchicine, could reduce the progression of AS. If positive, this trial will be the first to provide a potential therapeutic option for millions of people world-wide with AS.

Enrollment

150 estimated patients

Sex

All

Ages

50 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criterion:

• Asymptomatic moderate aortic valve stenosis on recent (<6 months) echocardiography (based on peak velocity, mean gradient, aortic valve area). The severity of AS will be quantified according to current EACVI / ASE guidelines.

Exclusion Criteria:

  • Heavily calcified aortic valve on echocardiography (defined as grade 4 calcification: extensive thickening/calcification of all cusps as described in the articles by Rosenhek et al.);
  • a planned aortic valve replacement in the next six months;
  • severe mitral valve stenosis (MVA < 1cm2);
  • severe mitral or aortic valve regurgitation;
  • rheumatic aortic valve disease;
  • bicuspid aortic valve;
  • valvular disease due to history of chest radiation;
  • left ventricular dysfunction (LVEF < 35%);
  • renal impairment (eGFR <30 ml/min/1.73m2);
  • patients aged <50 and >80 years;
  • pre-existing chronic gastro-intestinal complaints which may obscure signs of colchicine intolerance;
  • child-bearing potential without the use of contraception;
  • use of CYP3A4 (e.g. verapamil) or P-glycoprotein inhibitors;
  • use of bisphosphonate or denosumab;
  • chronic use of immunosuppressants or anti-inflammatory drugs including colchicine and NSAID's (excl. acetylsalicylic acid);
  • active or chronic liver disease;
  • the presence of a pacemaker or internal cardiac defibrillator;
  • life expectancy <2 years.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Quadruple Blind

150 participants in 2 patient groups, including a placebo group

Colchicine
Active Comparator group
Description:
75 patients will receive colchicine tablets
Treatment:
Drug: Colchicine
Placebo
Placebo Comparator group
Description:
75 patients will receive placebo tablets
Treatment:
Drug: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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