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Defining Robust Predictors of Chemotherapy Related Cardiotoxicity

University College London (UCL) logo

University College London (UCL)

Status

Enrolling

Conditions

Cardiotoxicity
Gastrointestinal Neoplasms

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Observational prospective cohort study designed for patients with gastrointestinal cancers receiving a fluoropyrimidine based chemotherapy regimen.

Full description

All enrolled participants will undergo baseline cardiovascular risk assessment (using QRISK3 and SCORE 2 risk calculators), cardiac, oncological and medication history. All participants will have serial cardiac symptom assessment, 12 lead ECG and cardiac biomarker assessments(high sensitivity troponin T and NT pro BNP) at baseline, on completion of the first cycle of treatment and post completion of treatment. Participants will be followed up for the development of cardiotoxicity.

Enrollment

600 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age >18
  • Consented to receive fluoropyrimidine chemotherapy for GI malignancies (gastro-oesophageal, colorectal, pancreatic)
  • Capacity to provide consent

Exclusion criteria

  • Age <18
  • Lacking capacity to consent

Trial contacts and locations

1

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Central trial contact

Aderonke Abiodun

Data sourced from clinicaltrials.gov

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