Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07528586

Serial Cardiac Magnetic Resonance Imaging (CMR) With Contrast Agents and Biomarker Analysis for the Detection of Cardiotoxicity Under Anthracycline-containing Cancer Therapy

Led by Robert Bosch Gesellschaft für Medizinische Forschung mbH (RBMF) · Updated on 2026-04-14

93

Participants Needed

1

Research Sites

208 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of the trial is the early detection of cardiotoxicity in patients treated with anthracycline-based chemotherapy. Current diagnostics, such as troponin T, NT-pro-BNP, electrocardiogram, and echocardiography, are not able to identify early myocardial damage. Therefore, this study aims to identify early myocardial damage by using cardiac magnetic resonance imaging. The primary endpoint of this study is the change in relaxation times in CMR before, during, and after therapy. Furthermore, the study analyzes: * other abnormal results in CMR * changes in troponin T and NT-pro-BNP * changes in global longitudinal strain in echocardiography and correlation with results of CMR * detection of new biomarkers in blood, urine, or stool

CONDITIONS

Official Title

Serial Cardiac Magnetic Resonance Imaging (CMR) With Contrast Agents and Biomarker Analysis for the Detection of Cardiotoxicity Under Anthracycline-containing Cancer Therapy

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients recommended for cancer treatment including at least four doses of anthracycline chemotherapy
Not Eligible

You will not qualify if you...

  • Unable to provide informed consent
  • Prior treatment with anthracyclines
  • Use of cardiotoxic drugs like high-dose cyclophosphamide, HER2 inhibitors, VEGF inhibitors, BCR-ABL inhibitors, BRAF inhibitors, MEK inhibitors, or immune checkpoint inhibitors within the last 6 months
  • Planned invasive heart procedures during the study
  • Heart involvement from other diseases such as amyloidosis
  • Receiving fewer than four anthracycline doses
  • Use of liposomal anthracycline formulations
  • Anthracyclines not given in every chemotherapy cycle
  • Prior chest radiation involving the heart before anthracycline treatment
  • Participation in another clinical trial currently or within the last 3 months
  • Kidney function below specified threshold (GFR < 30 ml/min/1.73 m²)
  • Around the time of liver transplantation surgery
  • Contraindications to cardiac MRI, including metallic implants like pacemakers
  • Pregnancy or breastfeeding
  • Allergy or intolerance to gadolinium-based contrast agents
  • Vulnerable populations such as individuals unable to consent or prisoners

AI-Screening

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Trial Site Locations

Total: 1 location

1

Robert Bosch Gesellschaft für Medizinische Forschung mbH

Stuttgart, Germany, 70376

Actively Recruiting

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Research Team

M

Matthias Prof. Dr. med. Schwab

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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