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NCT Number: NCT07372820

METABolic Deterioration in HTX Determines Outcomes

METAB-HTX is a prospective, longitudinal cohort study evaluating cardiac and systemic metabolism in heart transplant recipients.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

Bankground:

Heart Transplantation (HTS) is the treatment of choice for advanced heart failure, yet long-time survival rates require further improvement. Recent studies highlight obesity, type 2 diabetes, renal dysfunction, and hepatic impairment as key contributors to post-transplant mortality. Furthermore, critical questions persist in understanding the optimal metabolic surveillance post-HTX, the direct association between metabolic dysregulation and cardiac dysfunction, inter-organ interactions linking metabolic decline to hepatic/renal impairment and the timing of therapeutic strategies.

Therefore: METAB-HTX study aims to address these open questions, hypothesizing that metabolic deterioration post-HTX is associated with impaired cardiac function and survival.

Study Design:

The study employs advanced multi-modal phenotyping to investigate interactions between cardiac function, metabolic dysregulation, and systemic organ dysfunction.

Cardiac Phenotyping:

  • Imaging: Serial echocardiography, cardiac MRI (cMRI), and magnetic resonance spectroscopy (MRS) for myocardial structure, perfusion, and metabolic profiling.
  • Vascular Evaluation: Coronary angiography to detect macro- and microvascular coronary allograft vasculopathy (CAV).
  • Rejection Monitoring: Protocol-driven endomyocardial biopsies for histopathological grading.

Metabolic phenotyping:

  • Serial oral glucose tolerance tests, homeostasis model assessment, type 2 diabetes endotyping and muscle biopsies.
  • Advanced lipid panels, HDL functional assays and plasma membrane lipid fluidity analyses.
  • MRI/MRS-based quantification of adipose tissue distribution and ectopic fat deposition.

Systemic Organ Evaluation:

  • renal and liver function.

Molecular and Multi-Omics Integration:

  • Myocardial Energy Metabolism, Genomic/Transcriptomic Profiling, Thromoboinflammation and Neoplasia Risk.

This innovative study aims to bridge critical gaps in understanding post-transplant metabolic pathophysiology, potentially refining surveillance protocols and guiding targeted therapies to improve long-term survival through precision medicine strategies

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age: ≥ 18 years
  • Planned or already conducted heart transplantation
  • Informed consent

Exclusion criteria

  • Absence of informed consent

Treatment and study plan

Primary outcomes

  1. diastolic and systolic left ventricular function

    Time frame: Baseline, 1 year, and 2 years after heart transplantation

    in cardiac MRI or echocardiography

  2. CAV diagnosis

    Time frame: Baseline, 1 year, and up to 24 months

    coronary angiography, intravascular imaging and intravascular physiology measuraments

  3. Allograft rejection will be evaluated by endomyocardial biopsy

    Time frame: 1 year and 5 years after heart transplantation

    Tissue specimens will be collected from the interventricular septum and analyzed by cardiac transplant pathologists. Myocardial inflammation will be assessed in endomyocardial biopsies using immunohistochemistry followed by quantitative digital image analysis. Inflammatory cell infiltration will be quantified as the number of positive cells per square millimeter (mm²), providing a quantitative measure of myocardial inflammatory burden. In addition, biopsy tissue will be used for exploratory molecular analyses.

  4. Worsening of kidney function

    Time frame: Baseline, 1 year, and 2 years after heart transplantation

    Renal function will be assessed using estimated glomerular filtration rate (eGFR) as the primary quantitative measure. eGFR will be calculated from serum creatinine and cystatin C obtained from periodic blood sampling. Additional renal assessments, including duplex sonography, urinary markers, and immunological parameters, will be used for supportive and exploratory analyses.

  5. Infection requiring heath care professional interventions

    Time frame: Baseline, 1 year, and 2 years after heart transplantation

    clinical events, labs (CRP) , outpatient contact, hospitalisation.

  6. Diagnosis of malignencies

    Time frame: Baseline, 1 year, and 2 years after heart transplantation

    By whole-body CT scans, screening for occult blood within the stool and if indicated gastroscopy and coloscopy. Analysis of epigenetic alterations in leukocytes which are associated with post HTX events like neoplasia.

  7. Worsening of metabolic derangements

    Time frame: Baseline, 1 year, and 2 years after heart transplantation

    Changes in glucose and lipid metabolism, insulin resistance, HDL function, and body fat distribution will be assessed using blood tests, oral glucose tolerance, and imaging in selected participants.

  8. Liver deterioration

    Time frame: Baseline, 1 year, and 2 years after heart transplantation

    Liver structure and function will be assessed using blood tests (liver enzymes, bilirubin, albumin, INR), imaging (ultrasound, CT, transient elastography), and fibrosis scores (FIB-4) in selected participants.

Secondary outcomes

  1. Hospitalisation due to heart transplant events

    Time frame: up to 5 years (follow-up in clinical routine)

    Number of hospitalisations due to heart transplant-related events after study inclusion

  2. Cardiovascular mortality and all-cause mortality

    Time frame: up to 5 years (follow-up in clinical routine)

    Survival and clinical outcomes after study index visit (inclusion)

  3. Re-transplantation or ventricular assist device implantation

    Time frame: Through study completion, up to 5 years after heart transplantation

    Incidence of re-transplantation or ventricular assist device implantation during follow-up.

Study contacts

Contact information is provided by the study sponsor or research team.

Amin Polzin, Prof.

CONTACT

[email protected]

0211 81 18801

Fabian Voß, Dr. med.

CONTACT

[email protected]

02118118800

Sponsors and collaborators

Lead sponsor

Heinrich-Heine University, Duesseldorf

Other

Registry information

Official study title

METAB-HTX: Prospective, Longitudinal Cohort Study Evaluationg Cardiac and Systemic Metabolism After Heart Transplantation

Acronym: METAB-HTX

Important dates

Study start
2025
Primary completion
2030
Study completion
2032
First posted
Jan 28, 2026
Registry last updated
Jan 28, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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