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Strain sUrveillance during Chemotherapy for improving Cardiovascular OUtcomes

Strain sUrveillance during Chemotherapy for improving Cardiovascular OUtcomes

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-POR-17012742
Enrollment
Unknown
Registered
2017-09-19
Start date
2017-10-01
Completion date
Unknown
Last updated
2017-10-02

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

Conditions

malignant tumor

Interventions

Strain surveillance:drug therapy
Routine echocardiograpy:drug therapy

Sponsors

Affiliated Hospital of Jiangsu University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients actively undergoing chemotherapy at increased risk of cardiotoxicity; use of anthracycline WITH current (but not necessarily concurrent) rastuzumab (Herceptin) in breast-cancer with the HER2 mutation OR tyrosine kinase inhibitors (eg sunitinib) OR cumulative anthracycline dose >450g/m2 of doxorubicin, or equivalent other anthracycline cumulative dose (eg for epirubicin >900g/m2). OR increased risk of HF (any two of age >65y, type 2 diabetes mellitus, hypertension, previous cardiac injury eg. myocardial infarction); 2. Live within a geographically accessible area for follow-up; 3. Are able and willing to provide written informed consent to participate in the study (this includes the ability to communicate fluently with the investigator and that the patient is mentally competent).

Exclusion criteria

Exclusion criteria: 1. Unable to provide written informed consent to participate in this study; 2. Participating in another clinical research trial where randomized treatment would be unacceptable; 3. Valvular stenosis or regurgitation of >moderate severity; 4. History of previous heart failure (baseline NYHA >2); 5. Systolic BP <110mmHg; 6. Pulse <60/minute; 7. Inability to acquire interpretable images (identified from baseline echo); 8. Contraindications/Intolerance to beta blockers or ACE inhibitors; 9. Existing therapy with both beta blockers and ACE inhibitors; 10. Oncologic (or other) life expectancy <12 months or any other medical condition (including pregnancy) that results in the belief (deemed by the Chief Investigators) that it is not appropriate for the patient to participate in this trial.

Design outcomes

Primary

MeasureTime frame
myocardial strain;cardiac function;

Countries

China

Contacts

Public ContactYan Jin-Chuan

Affiliated Hospital of Jiangsu University

yanjinchuan@hotmail.com+86 13921594695

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026