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A clinical study of gene testing combined with proteomic analysis to evaluate the difference in clinical features and prognosis of patients with cardiomyopathy

A clinical study of gene testing combined with proteomic analysis to evaluate the difference in clinical features and prognosis of patients with cardiomyopathy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400086653
Enrollment
Unknown
Registered
2024-07-08
Start date
2024-07-10
Completion date
Unknown
Last updated
2024-07-15

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

Conditions

Cardiomyopathy

Interventions

Group with low cardiac markers:None
Cardiac markers high level group:None

Sponsors

The First Affiliated Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Patients who meet the 2023 European Society of Cardiology classification criteria for cardiomyopathy and the corresponding diagnostic criteria for cardiomyopathy guidelines; 2. Age 18-85; 3. The expected survival of the patients was greater than 12 months; 4. Patients with good compliance who volunteered for follow-up

Exclusion criteria

Exclusion criteria: 1. Unable to tolerate imaging evaluation of cardiac structure and function due to severe disease; 2. Have a history of drug abuse; 3. Blood biomarkers and imaging indicators cannot be reviewed regularly at follow-up visits; 4. End-stage renal failure (defined as glomerular filtration rate less than 15ml/min.m2)

Design outcomes

Primary

MeasureTime frame
All-cause death;Cardiovascular death;

Secondary

MeasureTime frame
All-cause rehospitalization;Cardiovascular rehospitalization;

Countries

China

Contacts

Public ContactYing Liu

The First Affiliated Hospital of Dalian Medical University

18098875801@163.com+86 180 9887 5801

Outcome results

None listed

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