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Follow-up Study of Discomfort Symptoms and Outcomes in Patients with Cardiovascular Diseases

Full-cycle Management of Discomfort Symptoms and Outcomes in Patients with Cardiovascular Diseases: A Prospective Observational Cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600127948
Enrollment
Unknown
Registered
2026-07-10
Start date
2026-07-10
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Cardiovascular diseases

Interventions

Follow-up Cohort of Discomfort Symptoms and Outcomes in Patients with Cardiovascular Diseases:None

Sponsors

Fuzhou University Affiliated Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients clinically diagnosed with cardiovascular disease and hospitalized in the study departments; 2.Patients who are able to understand the study content and complete questionnaire assessments; 3.Patients who voluntarily agree to participate in the study and provide written informed consent; 4.Patients who are able to cooperate with baseline assessments during hospitalization, collection of relevant objective clinical indicators, biospecimen collection, and long-term post-discharge follow-up;

Exclusion criteria

Exclusion criteria: 1.Patients with end-stage malignant tumors or other serious diseases, with a life expectancy of less than 1 year; 2.Patients with severe cognitive impairment, psychiatric disorders, impaired consciousness, or language/communication disorders that preclude understanding of the study content, completion of questionnaire assessments, or provision of informed consent; 3.Patients in critical condition for whom study-related assessments may substantially increase the patient burden; 4.Patients who have previously participated in other clinical trials that may have intervention conflicts with this study; 5.Other conditions deemed by the investigators to be unsuitable for inclusion in this study;

Design outcomes

Primary

MeasureTime frame
All-cause mortality;Major adverse cardiovascular events;

Secondary

MeasureTime frame
Treatment adherence;Quality of life;

Countries

China

Contacts

Public ContactJiinyi He

Fuzhou University Affiliated Provincial Hospital

hejinyi2010@126.com+86 591 8821 7370

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026