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Shizuoka Cardiovascular events Prospective Study

Shizuoka Cardiovascular events Prospective Study - SCOPE

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1040210102
Enrollment
200
Registered
2021-11-19
Start date
2021-12-22
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

Solid tumor

Interventions

None listed

Sponsors

Ko Ryo
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients with solid tumor who have received no prior chemotherapy or no more than two regimens of chemotherapy. 2) Anticancer therapy with regimens including immune checkpoint inhibitors or angiogenesis inhibitors (both antibody and tyrosine kinase inhibitors are acceptable) will be started within 28 days of enrollment. 3) At least 20 years old at the time of registration. 4) The treating investigator has determined that anticancer treatment is possible. 5) Survival of at least 24 weeks after enrollment is expected. 6) The patient's written consent to participate in the research has been obtained.

Exclusion criteria

Exclusion criteria: 1) Patients who are scheduled to receive only local or endocrine therapy as anticancer therapy. 2) Patients scheduled to receive chemoradiation therapy in which the chest area will be irradiated. 3) Patients with a history of treatment with immune checkpoint inhibitors or angiogenesis inhibitors. 4) Patients with acute coronary syndromes (myocardial infarction, angina pectoris), acute heart failure, or other urgent cardiac conditions that require treatment or procedures at the time of enrollment. 5) Patients with obvious cognitive decline or concomitant psychiatric disorders who are judged to be unable to participate in the study. 6) Patients who are judged by the treating investigators to be inappropriate to participate in this study for anti-cancer treatment.

Design outcomes

Primary

MeasureTime frame
Incidence of cardiac hypofunction

Secondary

MeasureTime frame
Incidence of cardiac hypofunction by drug Incidence of cardiac hypofunction by cancer type Relationship between other patient background and laboratory results at enrollment and incidence of cardiac hypofunction Incidence of symptomatic cardiac hypofunction Incidence of other cardiovascular events Status of treatment for cardiac hypofunction

Contacts

Public ContactRyo Ko

Shizuoka Cancer Center

r.ko@scchr.jp+81-55-989-5222

Outcome results

None listed

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