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A multicenter trial to assess transcatheter aortic valve replacement for chronic hemodialysis patients with aortic valve stenosis

A multicenter trial to assess transcatheter aortic valve replacement for chronic hemodialysis patients with aortic valve stenosis - Transcatheter aortic valve replacement for chronic hemodialysis patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000012426
Enrollment
20
Registered
2013-12-01
Start date
2013-12-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Severe aortic valve stenosis Chronic kidney disease (hemodialysis patients)

Interventions

Sponsors

Public interest incorporated foundation Ohara HealthCare Foundation Kurashiki Central Hospital Heart Disease Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients who have a high risk for operative mortality or are 'non-operable' as determined by cardiologist and cardiovascular surgeon 2.Severe aortic valve stenosis with the mean pressure gradient more than 40 mmHg, velocity more than 4.0 m/sec, or aortic valve area less than 0.8 cm2 by ultrasound cardiography 3.Heart failure symptoms with the NYHA classification greater than class II 4.Patient or substitute decision-maker signed the written informed consent, which had been approved by the institutional review board or its equivalence 5.Patient who is possible to visit on all follow-up days required after procedure

Exclusion criteria

Exclusion criteria: 1. Acute myocardial infarction within 1 month 2. Unicuspid, bicuspid aortic valve, or aortic valve stenosis without calcification 3. Severe aortic valve regurgitation 4. Cardiac intervention within 2 weeks 5. Prior valve surgery with artifical valve ring or severe mitral valve regurgitation with level 3 or 4 6. Leukopenia, acute anemia, thrombocytopenic purpura, or past history of coagulation disorder 7. Coronary artery disease with significant stenosis requiring intervention. 8. Unstable circulation requiring mechanical support 9. Emergency procedure for any reason 10. Obstructive or nonobstructive cardiomyopathy 11. Severe LV dysfunction (LVEF<20%) 12. Cardiac tumor, thrombus, vegetation in UCG 13. Active gastrointestinal ulcer or history of upper gastrointestinal bleeding within 3 months 14. Allergy to aspirin, heparin, ticropigin, or contrast medium 15. Aortic valve annulus smaller than 18 mm or larger than 25 mm 16. CVA or TIA within 1 month 17. Life expectancy less than 12 months due to non-cardiac disease 18. Involvement in another clinical trial 19. Active bacterial endocarditis or other active infections 20. Massive calcified cusp of aortic valve close to the coronary ostium 21. Allergy to cobalt-chromium alloy 22. Abdominal or thoracic aortic aneurysm or atheroma (diameters more than 5 cm ), and serious denaturation or anatomical features of thoracoabdominal aorta 23. Severe calcification, extreme tortuosity and vessel diameter less than 6 mm making the safe insertion of sheath introducer impossible from the common iliac artery through the femoral artery

Design outcomes

Primary

MeasureTime frame
Improvement of heart failure symptoms more than 1 grade in the NYHA classification at the postoperative 1st year

Countries

Japan

Contacts

Public ContactHarumi katoh

Kurashiki Central Hospital Department of Cardiology

kenkyu@kchnet.or.jp086-422-0210

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026