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The Efficacy and Safety for TAVR by Using Self-expandable Device in Dialysis Patients with Severe Aortic Stenosis

The Efficacy and Safety for Transcatheter Aortic Valve Replacement by Using Self-expandable Device in Dialysis Patients with Severe Aortic Stenosis - The Efficacy and Safety for TAVR by Using Self-expandable Device in Dialysis Patients with Severe Aortic Stenosis

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2032200010
Enrollment
10
Registered
2020-04-09
Start date
2020-04-09
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 stenosis aortic stenosis

Interventions

Transcatheter Aortic Valve Replacement by Using Self-expandable Device
TAVR

Sponsors

Saito Shigeru
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)The patients with severe aortic stenosis (AS) 2)The patients have AVA 40 mmHg or Peak aortic-jet velocity > 4.0 m/s in transthoratic echocardiograply at rest or dobtamin stress echocardiography. 3)The patients have symptomatic severe AS with >= NYHA class 2 4)The patients have high risk for surgical aortic valve replacement in heart team discussion 5)The patients with dialysis. The patients have performed maintained dialysis >= 1 month as stable. 6)The patients have performed maintained dialysis including either peritoneal dialysis or hemodialysis. 7)The patients >= 20 years old and >= 90 years old. 8)The patients agree this study and write informed consents after they understand this study protocol.

Exclusion criteria

Exclusion criteria: 1) The patients with low ejection fraction (less than 20%). 2) The patients with myocardial infarction within 30days. 3) The patients with fresh bleeding. 4) The patients with cerebral infarction within 6 months. 5) The patients with hemoglobin < 8.0 g/dl. 6) The patients with WBC <3000 or PLT < 100000. 7) The patients with positive HBV or HCV or HIV. 8) The patients with participate other clinical trial. 9) The patients with pregnant women (including possible) or lactating women 10) The patients that research director or contributory members judged inappropriate patients in this study. 11) The patients with need for emergency operation even if any reason. 12) The patients who have a life expectancy of less than 12 months due to comorbidities without cardiac disease.

Design outcomes

Primary

MeasureTime frame
The primary endpoint is all-cause death or major stroke at 12 months.

Secondary

MeasureTime frame
Major Adverse Cardiovascular and Cerebrovascular Event (MACCE) event rate. MACCE is defined as a composite of: All-cause death Myocardial infarction (MI) All stroke, and Reintervention 2) The occurrence of individual MACCE components. 3) Conduction disturbance requiring permanent pacemaker implantation 4) Cardiovascular deaths and valve-related deaths 5) Strokes (of any severity) and TIAs If the patients have any symptoms that are suspected for stroke, the patients are consulted and evaluated by neurologist. Head Magnetic Resonance Imaging (MRI) is planned to perform before and after procedure regardless of any symptoms. 6) Hospital stay 1 Hospital stay at 12 months 2 Length of index procedure hospital stay 3 Hospitalization related with aortic disease 4 Re-hospitalization after TAVR procedure 2 Change in NYHA class 3 Change in distance walked during 6-minute walk test (6MWT) 4 Quality of Life (QoL) change using the following measures: Kansas City Cardiomyopathy Questionnaire (KCCQ) SF-36 5 Echocardiographic assessment of valve performance (VARC 2) transvalvular mean gradient effective orifice area degree of aortic valve regurgitation (transvalvular and paravalvular) left ventricular mass index left ventricular global longitudinal strain pattern 6 Prosthetic Valve thrombosis and deformation of flame of prosthetic valve by the multislice CT at discharge, 1 year and annually up to 5 years 7 Device success defined as follows: Successful vascular access, delivery and deployment of the device, and successful retrieval of the delivery system, correct position of the device in the proper anatomical location (placement in the annulus with no impedance on device function), Intended performance of the prosthetic valve (mean aortic valve gradient < 20 mmHg or peak velocity < 3 m/sec, without moderate or severe prosthetic valve AR). 8 success rate of procedure defined as device success without MACCE

Contacts

Public ContactKoki Shishido

ShonanKamakura General Hospital

koki10192002@yahoo.co.jp+81-467-46-1717

Outcome results

None listed

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