NCT07332520

Brief Summary

This study aims to develop a better model to predict one-year risk of death in patients with heart failure. We will test whether combining information from routine blood tests (like NT-proBNP) and heart scans (measuring features like epicardial fat density) improves risk prediction compared to using either type of data alone. This is a retrospective study using existing medical records of patients treated for chronic heart failure at Xinjiang Medical University First Affiliated Hospital between 2012 and 2024. No new patient contact or interventions are involved. The goal is to enable more accurate, personalized risk assessment across different types of heart failure (HFrEF, HFmrEF, HFpEF).

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
4,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2012

Longer than P75 for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2012

Completed
13 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2024

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

January 31, 2025

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

December 28, 2025

Completed
15 days until next milestone

First Posted

Study publicly available on registry

January 12, 2026

Completed
Last Updated

January 27, 2026

Status Verified

January 1, 2026

Enrollment Period

13 years

First QC Date

December 28, 2025

Last Update Submit

January 26, 2026

Conditions

Keywords

Heart failure prognosisBiomarkersNT-proBNPMedical imagingEchocardiographyComputed tomographyEpicardial adipose tissueGlobal longitudinal strainRisk prediction modelRetrospective cohort studyHFpEFHFrEFPhenotypeAll-cause mortality

Outcome Measures

Primary Outcomes (1)

  • All-cause mortality

    Occurrence of death from any cause within one year (365 days) from the index date. The index date is defined as the date of the first qualifying encounter that meets all inclusion criteria.

    1 year

Secondary Outcomes (5)

  • Phenotype-specific prognostic performance

    1 year

  • Independent prognostic value of EAT density in HFpEF

    1 year

  • Occurrence of HFimpEF

    Through study completion,up to 13 years.

  • Association between baseline NT-proBNP level and HFimpEF

    Through study completion, up to 13 years.

  • Association between baseline EAT density and HFimpEF

    Through study completion, up to 13 years.

Study Arms (1)

Heart Failure Cohort

Adult patients (≥18 years) with a confirmed diagnosis of chronic heart failure who had both qualifying blood biomarker assessment and cardiac imaging performed within a specified window at the study center between 2012 and 2024. This is an observational cohort. No specific intervention is administered or withheld as part of the research protocol.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adults diagnosed with chronic heart failure at the study center between 2012 and 2024.

You may qualify if:

  • Age ≥ 18 years.
  • Confirmed diagnosis of chronic heart failure.
  • Treated at the study center between January 1, 2012, and December 31, 2024.
  • Availability of both qualifying blood biomarker test results (NT-proBNP and/or high-sensitivity cardiac troponin) and cardiac imaging (echocardiography and/or cardiac CT) performed within a ±3-month window around the index encounter.

You may not qualify if:

  • Heart failure primarily due to severe primary valvular disease, acute myocardial infarction, myocarditis, or pulmonary embolism.
  • End-stage renal disease requiring dialysis.
  • Clinical records or follow-up data are severely incomplete, precluding outcome assessment.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Heart FailureHeart Failure, SystolicHeart Failure, Diastolic

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular Diseases

Study Officials

  • Xiang Xie, PhD

    First Affiliated Hospital of Xinjiang Medical University

    STUDY CHAIR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

December 28, 2025

First Posted

January 12, 2026

Study Start

January 1, 2012

Primary Completion

December 31, 2024

Study Completion

January 31, 2025

Last Updated

January 27, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share