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Left Ventricular Reverse Remodeling Trajectories and Their Predictors in Patients with Heart Failure and Reduced Ejection Fraction on Guideline-Directed Medical Therapy:A Retrospective Cohort Study

Left Ventricular Reverse Remodeling Trajectories and Their Predictors in Patients with Heart Failure and Reduced Ejection Fraction on Guideline-Directed Medical Therapy:A Retrospective Cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600117762
Enrollment
Unknown
Registered
2026-01-28
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Heart failure

Interventions

Rapid Reverse Engineering and Refactoring Group:N/A
Slow or no reverse reconstruction group:N/A

Sponsors

The First Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >= 18 years; 2.Clinical diagnosis of heart failure meeting the criteria of the *2022 AHA/ACC/HFSA Heart Failure Management Guideline; 3.Initiation or first optimization of Guideline-Directed Medical Therapy during the index hospitalization, including at least two drug classes among: beta-blockers, renin-angiotensin system inhibitors, mineralocorticoid receptor antagonists, and SGLT2 inhibitors; 4.Baseline echocardiography (performed prior to or concurrently with GDMT initiation/optimization) with standardized measurement (preferably Simpson‘s biplane method) confirming a left ventricular ejection fraction (LVEF) =30 days after initiation/optimization and discharge), with both examinations occurring after the efficacy observation start point (3 months post-stabilization) and an inter-examination interval of >=1 month;

Exclusion criteria

Exclusion criteria: 1.Missing or poor-quality echocardiographic data at baseline or during follow-up precluding accurate measurement of LVEF and left ventricular dimensions; 2.Conditions severely interfering with cardiac structure and function assessment (including but not limited to: severe valvular disease without intervention, acute myocardial infarction within 3 months prior to enrollment, constrictive pericarditis, history of heart transplantation or left ventricular assist device implantation); 3.Severely missing clinical follow-up data, preventing assessment of GDMT adherence; 4.End-stage renal disease with long-term dependence on renal replacement therapy; 5.Pregnancy or lactation

Design outcomes

Primary

MeasureTime frame
Left Ventricular Reverse Remodeling Trajectory Classification;

Secondary

MeasureTime frame
Heart failure readmission;Composite endpoint (Heart failure readmission or All-cause mortality);All-cause mortality;

Countries

China

Contacts

Public ContactWang yushi

The First Hospital of Jilin University

yushi@jlu.edu.cn+86 431 8878 2417

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026