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Clinical Trials/NCT06702436
NCT06702436CompletedNot Applicable

Impact of Treatment Approaches on Mortality in Cancer Patients With Non-ST Elevation Myocardial Infarction: Invasive vs. Conservative Strategies

Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital1 site in 1 country12,500 target enrollmentStarted: June 1, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
12,500
Locations
1
Primary Endpoint
hospital mortality

Study Overview

Brief Summary

This retrospective study investigates the impact of invasive versus conservative management strategies in cancer patients presenting with non-ST elevation myocardial infarction (non-ST MI). Patients aged 18 and older, who were treated for non-ST MI in a hospital setting and had a confirmed cancer diagnosis, are included. The primary outcome is hospital mortality, assessed using GRACE scores to evaluate mortality risk. Patients are grouped based on their received interventions-either invasive (including coronary angiography and revascularization) or pharmacological treatment. Risk factors contributing to mortality, such as cancer type, metastasis presence, comorbidities, and laboratory findings, will also be analyzed to better understand the interplay of oncologic and cardiovascular conditions in this population.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age: Patients aged 18 years and older.
  • •Diagnosis: Patients with a confirmed cancer diagnosis.
  • •Acute Condition: Patients diagnosed with non-ST elevation myocardial infarction (non-ST MI).
  • •Treatment: Patients who received either invasive treatment (including coronary angiography and revascularization) or conservative (pharmacological) treatment for non-ST MI.
  • •Consent: Patients who have provided informed consent or are part of a retrospective study where consent is waived.

Exclusion Criteria

  • •Age: Patients younger than 18 years.
  • •Non-cancer diagnoses: Patients without a cancer diagnosis.
  • •ST-Elevation Myocardial Infarction: Patients with ST elevation myocardial infarction (STEMI) instead of non-ST elevation myocardial infarction (NSTEMI).
  • •Pre-existing severe comorbidities: Patients with severe or terminal comorbidities (e.g., end-stage liver disease, end-stage renal disease, or severe cognitive impairment) that would confound the outcomes.
  • •Incomplete medical records: Patients with missing data on relevant clinical variables (e.g., GRACE score, treatment received, or mortality data).
  • •Pregnancy: Pregnant patients, as their conditions may complicate the interpretation of results.
  • •Inability to provide informed consent: Patients unable to provide informed consent (if applicable).

Outcomes

Primary Outcomes

hospital mortality

Time Frame: From the date of hospital admission for NSTEMI until the occurrence of mortality, cardiovascular events, or hospital discharge, assessed up to 30 days.

Hospital mortality rate in cancer patients with non-ST elevation myocardial infarction, comparing invasive and conservative treatment strategies

Secondary Outcomes

  • Length of hospital stay:(From the date of hospital admission for NSTEMI until the occurrence of mortality, cardiovascular events, or hospital discharge, assessed up to 100 days.)
  • Re-hospitalization rate(The time frame for assessing re-hospitalization is from the date of hospital discharge to 100 days post-discharge)

Investigators

Sponsor
Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Arif Timuroğlu, MD

Principal Investigator

Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital

Study Sites (1)

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