Clinical trial Recruiting at 1 site Observational

Understanding heart failure through detailed patient profiles and molecular profiling

Official title: Molecular Underpinnings of Heart Failure, Integrative Multi-Omics, and Non-Coding RNA Profiling: the BIOCARDIUM-HF Study

Run by University of Zurich · NCT07158086 · Data updated 2026-11-12

This study tests whether combining clinical data with multi-omics profiling can reveal molecular signatures and non-coding RNAs linked to heart failure in adults.

Quick facts

Study typeObservational
SexAll
Enrollment500 (estimated)
SponsorUniversity of Zurich
Academic / other
Drugs / interventionschemotherapy, immunotherapy
Locations1 site (Zurich)
StatusRecruiting
StartedFebruary 1, 2025
Main results expectedNovember 30, 2030
Study endsNovember 30, 2031
Registry record updatedSeptember 25, 2026
Trial IDNCT07158086 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (18+) with a diagnosis of heart failure who can understand the study requirements and consent, and who are willing to participate in follow-up assessments.

Probably not a fit

Patients who do not develop measurable molecular signatures or biomarkers linked to progression may not benefit directly.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study collects comprehensive clinical data and deep molecular data from participants with heart failure to identify molecular patterns associated with disease onset and progression. It uses multi-omics approaches such as transcriptomics, epigenomics, and proteomics, along with imaging, hemodynamic data, and biomarker analyses, to create deep phenotypes. The goal is to find biomarkers that predict progression and to identify potential new therapeutic targets for future treatment strategies. Participants will undergo follow-up assessments and sample collection as part of routine clinical evaluation. The study is led by the University of Zurich at the University Hospital Zurich, with no listed collaborators.

Why it matters

Potential benefit: Participants may contribute to advances in understanding heart failure biology and potential future biomarker-guided strategies for prediction and treatment.

How similar studies have gone: Earlier studies using multi-omics in heart failure have shown promise in identifying molecular patterns, but this specific integrative approach is part of ongoing exploration.

Who can join: the full rules

Show full inclusion / exclusion criteria
INCLUSION CRITERIA

* Female and Male, age ≥18 years at screening.
* Diagnosis of Heart Failure according to ESC Heart Failure Guidelines
* Ability to understand the requirements of the study and to provide informed consent.
* Willingness to undergo follow-up.

EXCLUSION CRITERIA

Patients will be excluded if they meet any of the following conditions:

* Active malignancy or history of cancer with ongoing treatment (e.g., chemotherapy, radiotherapy, immunotherapy).
* Autoimmune or systemic inflammatory diseases.
* Concomitant infections, including acute systemic infections (e.g., sepsis, pneumonia) or chronic infections with systemic impact (e.g., HIV, hepatitis B/C with elevated transaminases).

Other exclusion criteria:

* Age\<18 years old
* Inability to provide written informed consent

Where it's running

  • University Hospital of Zurich
    Zurich, Switzerland
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.