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Assessment of anti-thrombotic effects of conventional anti-thrombotic therapy using total thrombus-formation analysis system in transcatheter aortic valve replacement

AFTER: Assessment oF anti-Thrombotic Effects of conventional anti-thrombotic therapy using total thrombus-formation analysis system in transcatheter aortic valve Replacement - AFTER

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000041165
Enrollment
120
Registered
2020-08-01
Start date
2020-06-25
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

Aortic stenosis

Interventions

None listed

Sponsors

Teikyo University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who can undergo TAVI via transfemoral approach

Exclusion criteria

Exclusion criteria: Patients who met the following criteria were excluded from this study; 1) TAVI using alternative access, 2) patients who cannot take anti-thrombotic therapy prior to TAVI, 3) TAVI needed more than two valve, 4) TAVI needed emergent surgical conversion, 5) new-onset atrial fibrillation, 6) TAVI in SAV, 7) patients refused to participate this study.

Design outcomes

Primary

MeasureTime frame
Anti-thrombotic abilities

Secondary

MeasureTime frame
Mortality, bleeding events, thrombotic events

Countries

Japan

Contacts

Public ContactHirofumi Hioki

Teikyo University Department of Internal Medicine, Division of Cardiology

hioki.teikyo@gmail.com0339641211

Outcome results

None listed

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