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REWARDS Premier Taxus-Liberte vs Xience V

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MedStar Health

Status

Completed

Conditions

Coronary Artery Disease

Treatments

Other: Observational

Study type

Observational

Funder types

Other

Identifiers

NCT02256527
REWARDS Premier TLX

Details and patient eligibility

About

Multicenter, retrospective registry to collect baseline, clinical, procedural, in hospital and 9-12 month follow-up data to compare major adverse cardiac events in patients receiving Promus Premier drug eluting stent to data already collected from the REWARDS-TLX Registry in which patients received either the Taxus Liberte or XIENCE V drug eluting stent.

Enrollment

917 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients 18 years of age or older
  • Underwent PCI with Promus Premier (alone) DES

Exclusion criteria

  • Underwent PCI with a non-Promus Premier DES during the same index procedure
  • Patients not taking, or unable to take, dual antiplatelet therapy (aspirin plus clopidogrel, prasugrel, or ticagrelor)

Trial design

917 participants in 1 patient group

Promus Premier
Description:
observational data
Treatment:
Other: Observational

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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