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New Biomarkers in the Prediction of Chemotherapy-induced Cardiotoxicity.

New Biomarkers in the Prediction of Chemotherapy-induced Cardiotoxicity.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05992337
Enrollment
200
Registered
2023-08-15
Start date
2021-09-01
Completion date
2025-01-31
Last updated
2023-08-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiotoxicity, Chemotherapy Effect, Chemotherapy Induced Systolic Dysfunction

Brief summary

Early detection and thus rapid therapy of cardiotoxicity related to chemotherapy are essential for restoring cardiovascular function. The complete recovery of the cardiovascular system decreases with time to identify the presence of cardiotoxic damage. The project aims to define new biomarkers for the early detection of cardiotoxicity in patients treated with chemotherapy.

Detailed description

The most effective approach to minimizing the consequences of cardiotoxicity of oncological treatment is its early identification, adjustment of oncological treatment (change of procedure, dose, drugs), and immediate initiation of cardiovascular therapy. However, the current standard for monitoring the cardiovascular system in cancer patients identifies cardiotoxicity only if functional impairment has already occurred, which precludes any chance of effective prevention. The aim of the project is to identify new biomarkers for the early detection of the cardiotoxic effect of chemotherapy in women with breast cancer.

Interventions

DIAGNOSTIC_TESTBlood sampling

Blood sample collection for mRNA determination

DIAGNOSTIC_TESTEchocardiography

Echocardiography for detection of ventricular dysfunction

DIAGNOSTIC_TESTCardio MRI

MRI for early detection of myocardial impairment caused by chemotherapy

DIAGNOSTIC_TEST24-hours monitoring of ECG

Diagnostic test for detection of arrhythmias as a consequence of cardiotoxicity

DIAGNOSTIC_TEST24 hours monitoring of BP

Diagnostic test for detection of hypertension as a consequence of cardiotoxicity

Sponsors

BioVendor LM
CollaboratorUNKNOWN
Oncology Center Medicon
CollaboratorUNKNOWN
Cardiology Prague
Lead SponsorNETWORK

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Breast cancer * Chemotherapy with a known cardiotoxic side effect

Exclusion criteria

* Known cardiovascular disease

Design outcomes

Primary

MeasureTime frameDescription
Early detection of the cardiotoxic effect of chemotherapy using new biomarkersone year follow-up.Echocardiography and MRI detection of cardiotoxic effect of chemotherapy - dysfunction of left ventricle, arrythmias, hypertension

Countries

Czechia

Contacts

Primary ContactRobert Petr, MD.
robert.petr81@gmail.com+420 233 336 334

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026