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Detection and Prevention of Cancer-Related Cardiovascular Toxicity Registry

U

University of Bologna

Status

Enrolling

Conditions

Cancer Related Cardiovascular Toxicity

Treatments

Combination Product: Prospective validation of the HFA-ICOS risk score in a subset of subjects with newly diagnosed breast cancer and undergoing treatment with anthracyclines analogues with or without radiotherapy

Study type

Observational

Funder types

Other

Identifiers

NCT06086132
ISACS CARDIONCO-PREDICT

Details and patient eligibility

About

This study is being done in order to assess the cardiovascular events known as cardiovascular toxicity of chemotherapy agents and radiotherapy protocols in cancer subjects to identify risk prediction, prevention and treatment of cancer therapy-related cardiovascular toxicity and cancer therapy-related cardiac dysfunction

Enrollment

10,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18 years old or older
  • Capable of giving informed consent
  • Diagnosis of cancer scheduled for treatment according to treating physician's discretion
  • Life expectancy >1 year
  • For the prospective validation of HFA-ICOS risk score validation: Newly diagnosed breast cancer undergoing treatment with anthracyclines analogues with or without radiotherapy, with or without trastuzumab, or other anticancer drugs

Exclusion criteria

  • Age <18 years old
  • Not able to give informed consent
  • Life expectancy <1 year
  • Advanced-stage cancer not eligible for treatment (subjects with an indication of palliative care) according to treating physician's

Trial design

10,000 participants in 2 patient groups

Breast cancer
Description:
Newly diagnosed breast cancer undergoing treatment with anthracyclines analogues with or without radiotherapy, with or without trastuzumab, or other anticancer drugs. (Non-interventional prospective patient registry)
Treatment:
Combination Product: Prospective validation of the HFA-ICOS risk score in a subset of subjects with newly diagnosed breast cancer and undergoing treatment with anthracyclines analogues with or without radiotherapy
Female and Male
Description:
Diagnosis of cancer scheduled for treatment according to the treating physician's discretion. (Non-interventional patient registry)

Trial contacts and locations

5

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Central trial contact

Maria Bergami; Edina Cenko

Data sourced from clinicaltrials.gov

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