Monitoring and analysis of continuous dynamic physiological data and prediction model of adverse cardiovascular events in patients with acute heart failure during hospitalization

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2200055863

Enrollment

Unknown

Registered

2022-01-21

Start date

2021-07-01

Completion date

Unknown

Last updated

2023-07-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

acute heart failure

Interventions

1:Cardiology patients wear SensEcho wearable physiological parameter monitoring system

Eligibility

Sex/Gender

All

Age

18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patients with acute heart failure; 2. 18-90 years old; 3. No further increase in troponin level; 4. No new arrhythmias or electrocardiogram changes in the past 8 hours; 5. No history of mental illness or other serious acute or chronic diseases; 6. Informed consent and signing an agreement to participate in this study.

Exclusion criteria

Exclusion criteria: 1. Uncontrolled unstable angina pectoris; 2. uncontrolled severe arrhythmias that cause symptoms or hemodynamic disorders; 3. Severe limb motor dysfunction; 4. Patients who do not cooperate or cannot communicate; 5. With severe physical illness and uncorrected clinical conditions (e.g., severe anemia, electrolyte disorder, and thyroid gland) Hyperfunction); 6. Participants in other clinical trials; 7. The expected survival time is less than 24 h.

Design outcomes

Primary

Measure	Time frame
Exercise capacity;Respiratory pattern;	—

Countries

China

Contacts

Public ContactPengming Yu

West China Hospital of Sichuan University

13438201451@126.com13438201451

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026