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NCT07332520: BIOPHF

Predicting Heart Failure Outcomes With Biomarkers and Imaging

Completed Last updated 27 January 2026
What this trial tests

trial in Heart Failure in 4,000 participants. Completed in 31 January 2025.

Timeline
1 January 2012
Primary endpoint
31 December 2024
31 January 2025

Quick facts

Lead sponsorXinjiang Medical University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment4,000
Start date1 January 2012
Primary completion31 December 2024
Estimated completion31 January 2025

Conditions studied

Sponsor

Xinjiang Medical University

Who can join

18 and older, any sex, with Heart Failure or Heart Failure, Systolic. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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).

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Heart Failure

Currently open trials in the same condition.

Other Xinjiang Medical University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07332520.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing