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HeartLogic study

A multicenter collaborative study to explore the effectiveness of HeartLogic in the management of heart failure

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1050250010
Enrollment
400
Registered
2025-04-28
Start date
2025-04-28
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

heart failure Cardiac Failure

Interventions

None listed

Sponsors

Oka Takafumi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - The study subjects who do not refuse to participate in the study by disclosing information about the study on the website or posters of each collaborating institution as an opt-out. - Persons who are at least 18 years old and residing in Japan at the time of obtaining consent. - Persons with a HeartLogic index who are ready for remote monitoring by LATITUDE NXT.

Exclusion criteria

Exclusion criteria: - Investigators who refuse to participate in this study by viewing information about this study on each collaborating institution's website or posters as an opt-out.

Design outcomes

Primary

MeasureTime frame
To evaluate the rate of rehospitalization for heart failure, the rate and incidence of heart failure events, death from cardiac causes, and death from all causes before and after HeartLogic activation

Secondary

MeasureTime frame
1. Correlate the rate of change or absolute value of HeartLogic index values with heart failure events and life expectancy. 2. Sensitivity and specificity of HeartLogic for heart failure hospitalizations analyzed by ROC analysis 3. Correlation of Heart Failure events and life expectancy by whether or not HeartLogic alert notifications are responded to after facility recognition 4. Number of alerts, follow-up period, etc. by total subjects, ICD, and CRT-D

Contacts

Public ContactTakafumi Oka

Osaka University Hospital

oka.takafumi.med@osaka-u.ac.jp+81-6-6879-3640

Outcome results

None listed

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