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A cohort study of anthracycline-induced cardiotoxicity

A cohort study of anthracycline-induced cardiotoxicity - A cohort study of anthracycline-induced cardiotoxicity

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000022984
Enrollment
500
Registered
2016-08-01
Start date
2016-08-01
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

All patients scheduled for anthracycline-containing therapy for various kinds of tumors

Interventions

Echocardiac examination (before &amp
during anthracycline treatment, after 3, 6, 9, 12, 18, 24 month)

Sponsors

University of Tsukuba
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) malignancy patients in the face of with anthracycline chemotherapy 2) age more than 20 years old 3) EF > 50% 4) life expectancy of > 1year 5) written informed consent

Exclusion criteria

Exclusion criteria: 1) cases with valuvular heart disease, gongenital heart disease, and cardiomyopathy 2) pregnant or lactating women 3) psychotic disorder

Design outcomes

Primary

MeasureTime frame
The incidence of cardiotoxicity defined as a reduction in left ventricular ejection fraction (LVEF) >10 percentage points from baseline and <50%

Secondary

MeasureTime frame
All cause death, the following cardiac events (cardiac death, acute pulmonary edema, acute coronary syndromes, llife-threatening arrhythmias), the recovery from cadiotoxicity after the initiation of heart failure treatment defined as EF>50%

Countries

Japan

Contacts

Public ContactKazuko Tajiri

University of Tsukuba Hospital Cardiovascular Division

ktajiri@md.tsukuba.ac.jp029-853-3143

Outcome results

None listed

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