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Bare Metal Stents and Drug Eluting Stents in Patients Who Underwent Blood Transfusion (TFPCI2)

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Samsung Medical Center

Status

Completed

Conditions

Percutaneous Coronary Intervention
Revascularization
Erythrocyte Transfusion

Treatments

Device: Stent, red blood cell transfusion

Study type

Observational

Funder types

Other

Identifiers

NCT03788148
SMC 2017-11-132

Details and patient eligibility

About

Retrospective cohort study of Korean National Healthcare Insurance Database. To investigate clinical outcomes of bare metal stents versus drug eluting stents in patients who underwent periprocedural red blood cell transfusion.

Full description

A Korean nationwide, multi-center, retrospective observational cohort study.

The receipt of red blood cell transfusion is at high risk of cardiac events or death. But little is know regarding the comparative outcomes of BMS and DES implantation in patients who underwent periprocedural red blood cell transfusion.

Longitudinal data is collected from administrative claims in the national health insurance services of Korea. All Korean data(N=500,591) undergoing PCI from 2006 to 2015 is extracted. BMS or DES Patients(N=28,322) who received periprocedural red blood cell transfusion is investigate. Clinical outcomes until December 31, 2017 is investigate.

Primary endpoint is a time to the first major adverse clinical event(MACE) defined as a composite of all-cause death, revascularization, critically ill cardiovascular status, or stroke.

Enrollment

28,322 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with percutaneous coronary intervention from 2006 to 2015
  • Patients with the implantation of BMS or DES
  • Patients with the receipt of periprocedural red blood cell transfusion

Exclusion criteria

  • Patients without any of stent implantation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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