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Prospective Registry of STable Angina RehabiliTation: Pilot Study

Not Applicable
Recruiting
Conditions
Stable coronary artery disease
Registration Number
JPRN-UMIN000045415
Lead Sponsor
Kyoto Prefectural University of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
50
Inclusion Criteria

Not provided

Exclusion Criteria

1. Acute coronary syndrome, including unstable angina with CCS classification IV 2. Three-vessel coronary artery disease 3. Left main coronary artery disease 4. Myocardial infarction within 6 months 5. Coronary artery revascularization within 6 months 6. Contraindication to antiplatelets 7. Left bundle branch block or Wolff-Parkinson-White syndrome 8. NYHA class III-IV heart failure at entry or hospitalization for exacerbation of heart failure within 6 months 9. Left ventricular ejection fraction < 35% 10. Pulmonary hypertension requiring drug therapy 11. Moderate or severe valvular heart disease or previous surgical/percutaneous treatment for valvular heart disease 12. Dilated or hypertrophic cardiomyopathy 13. Moderate or severe aortic aneurysm 14. Cardiac implantable electronic device including pacemaker, implantable cardioverter defibrillator, or biventricular pacemaker implantation 15. Left or right ventricular assist device or heart transplantation 16. Unable to exercise due to musculoskeletal disease or peripheral arterial disease 17. Terminal illness 18. Pregnant or lactating women 19. Estimated glomerular filtration rate <30 mL/min/1.73 m2, maintenance dialysis, peritoneal dialysis, or post-renal transplantation 20. Severe dementia 21. Home is far away from an outpatient cardiac rehabilitation center 22. Participating in another clinical trial involving interventions 23. Treating physician judged it inappropriate to participate in the study 24. Do not understand the Japanese language 25. Study researchers and their family members

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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