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Clinical Trials/NL-OMON37774
NL-OMON37774
Completed
Not Applicable

Early detection and prediction of cardiotoxicity in breast cancer patients treated with chemotherapy using the high sensitivity troponin T assay. - Use of high sensitivity troponin t to detect and predict cardiotoxicity

Maxima Medisch Centrum0 sites40 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
cardiotoxicity
Sponsor
Maxima Medisch Centrum
Enrollment
40
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Observational invasive

Investigators

Sponsor
Maxima Medisch Centrum

Eligibility Criteria

Inclusion Criteria

  • \-Female breast cancer patients
  • \-Age between 30\-60 years
  • \-18\-weeks of chemotherapy\-treatment, adjuvant or neo\-adjuvant
  • \-Chemotherapy may include: (AC) adriamycin/cyclophosphamide, (FEC) fluorouracil/epiribicin/cyclophosphamide, (TAC) taxotere/ adriamycin/cyclophosphamide
  • \-Ejection fraction \> 50%

Exclusion Criteria

  • \-Ejection fraction \<50%
  • \-previous signs of cardiovascular disease
  • \-kidney dysfunction (eGFR \<60 ml/min/1,73m^2\).
  • \-previous treatment with anthracyclines

Outcomes

Primary Outcomes

Not specified

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