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Cohort Study of Chronic Heart Failure

Cohort Study of Chronic Heart Failure

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06092658
Enrollment
20000
Registered
2023-10-23
Start date
2012-11-20
Completion date
2022-07-14
Last updated
2023-10-23

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

Conditions

Analyze Etiology, Comorbidities, Clinical Characteristics

Brief summary

The purpose is to understand the clinical characteristics of chronic heart failure as soon as possible, analyze the etiology, comorbidities, clinical characteristics, and treatment of heart failure patients, observe the gap between real-world clinical practice and guideline recommendations, and provide reference for the improvement of heart failure prevention and treatment in China.

Detailed description

Inclusion criteria: 1. Accompanied by difficulty breathing, fatigue, or decreased activity tolerance; 2. Signs of fluid retention (pulmonary congestion and peripheral edema); 3. Echocardiography shows abnormalities in cardiac structure and/or function; 4. Elevated levels of natriuretic peptide: B-type natriuretic peptide (BNP)\>35 ng/L and/or N-terminal B-type proBNP (NT proBNP)\>125 ng/L. 5. HF hospitalization recorded within the previous 12 months Exclusion criteria: 1. Concomitant severe liver function, renal failure, or other severe system dysfunction 2. Poor compliance, inability to obtain information, or voluntary refusal to participate in this study.

Interventions

OTHERNo Intervention

no intervention

Sponsors

Xiang Xie
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
19 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

1. Accompanied by difficulty breathing, fatigue, or decreased activity tolerance; 2. Signs of fluid retention (pulmonary congestion and peripheral edema); 3. Echocardiography shows abnormalities in cardiac structure and/or function; 4. Elevated levels of natriuretic peptide: B-type natriuretic peptide (BNP)\>35 ng/L and/or N-terminal B-type proBNP (NT proBNP)\>125 ng/L.

Exclusion criteria

1. Concomitant severe liver function, renal failure, or other severe system dysfunction 2. Poor compliance, inability to obtain information, or voluntary refusal to participate in this study.

Design outcomes

Primary

MeasureTime frameDescription
echocardiogramFollow up will be conducted at baseline, 6 months, 12 months, and 36 monthsejection fraction,Consider heart failure when the ejection fraction is less than 50%
cardiac markerFollow up will be conducted at baseline, 6 months, 12 months, and 36 monthsCK,CK-MB,cTnT,cTnI,Mb
serum biochemical indicatorsFollow up will be conducted at baseline, 6 months, 12 months, and 36 monthsHDL-cholesterol, mg/dL,LDL-cholesterol, mg/dL,Total cholesterol, mg/dL,Triglycerides, mg/dL

Secondary

MeasureTime frameDescription
Thyroid FunctionFollow up will be conducted at baseline, 6 months, 12 months, and 36 monthsthyroid hormone,Thyroid hormone blood testing: This is the most commonly used method to measure thyroid hormone levels in the blood. Common thyroid hormone indicators include thyroxine, free thyroxine, triiodothyronine, and free triiodothyronine.
Coagulation function indicatorsFollow up will be conducted at baseline, 6 months, 12 months, and 36 monthsD-Dimer
Blood routineFollow up will be conducted at baseline, 6 months, 12 months, and 36 monthsRBC

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026