Evaluating heart health in adult survivors of childhood cancer
Official title: Prospective Single Center Cohort Study for Early Detection of Cardiac Dysfunction in Childhood Cancer Survivors
Run by University of Bern · NCT03790943 · Data updated 2026-11-12
This study is testing if a new heart imaging technique can find heart problems earlier in adult survivors of childhood cancer who had treatments that might have harmed their hearts.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 500 (estimated) |
| Sponsor | University of Bern Academic / other |
| Drugs / interventions | chemotherapy, radiation |
| Locations | 6 sites (Basel, Canton of Basel-City and 5 other locations) |
| Status | Recruiting |
| Started | February 13, 2018 |
| Main results expected | April 23, 2029 |
| Study ends | April 23, 2029 |
| Registry record updated | May 29, 2026 |
| Trial ID | NCT03790943 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adult survivors of childhood cancer who were diagnosed before age 20 and have survived at least 5 years since their last cancer treatment.
✕Probably not a fit
Patients who were not treated with cardiotoxic therapies or who are not survivors of childhood cancer may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This multicenter, prospective cohort study assesses early cardiac dysfunction in adult survivors of childhood cancer using advanced echocardiographic techniques. The study aims to determine if speckle tracking echocardiography can detect cardiac dysfunction earlier than conventional methods. Participants will undergo a comprehensive cardiac evaluation, including both standard and novel echocardiographic assessments, as well as cardiopulmonary exercise testing. The focus is on survivors who received cardiotoxic treatments, such as anthracyclines or chest radiation, to identify those at higher risk for cardiac issues.
Why it matters
Potential benefit: If successful, this study could lead to earlier detection and intervention for cardiac dysfunction in childhood cancer survivors, potentially improving their long-term health outcomes.
How similar studies have gone: Other studies have shown promising results using advanced echocardiographic techniques for early detection of cardiac issues, suggesting this approach may be effective.
Who can join: the full rules
Show full inclusion / exclusion criteria
This prospective cohort study is nested within the Childhood Cancer Registry (ChCR), a national, population-based cancer registry that includes all children and adolescents in Switzerland who were diagnosed with cancer at age 0-20 years. It includes patients diagnosed with leukemia, lymphoma, central nervous system tumors, and malignant solid tumours or Langerhans cell histiocytosis. Childhood cancer survivors have survived at least 5 years from cancer diagnosis. Inclusion Criteria: * Registered in the ChCR * Formerly treated at the Department of Pediatric Hematology/Oncology of one of five participating centers * Treated with any chemotherapy and/or chest radiation * Survived ≥ 5 years since most recent cancer diagnosis (primary cancer, relapse(s), secondary cancer) at time of examination * Diagnosed at age ≤ 20 years * ≥ 18 years of age at time of study participation * Resident in Switzerland * Written informed consent Exclusion Criteria: * Study participants will be excluded if they do not meet the above mentioned inclusion criteria or refuse to participate in the study.
Where it's running
-
Department of Cardiology, University Hospital Basel
Basel, Canton of Basel-City, Switzerland Recruiting -
Department of Cardiology, Inselspital Bern
Bern, Switzerland Recruiting -
Department of Cardiology, University Hospitals of Geneva
Geneva, Switzerland Recruiting -
Department of Cardiology, Lucerne Cantonal Hospital
Lucerne, Switzerland Recruiting -
Department of Cardiology, Cantonal Hospital of St. Gallen
Sankt Gallen, Switzerland Recruiting -
Institute of Social and Preventive Medicine, University of Bern
Bern, Canton of Bern, Switzerland Active not recruiting
Study contacts
- Principal investigator: Claudia E Kuehni, MD — University of Bern
- Study coordinator: Claudia E Kuehni, MD
- Email: claudia.kuehni@unibe.ch
- Phone: +41 31 684 35 07
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.