Mode
Text Size
Log in / Sign up
N/A Completed N=4,182

PLATINUM Diversity

Source: ClinicalTrials.gov NCT02240810 ↗
Enrolled (actual)
4,182
Serious AEs
10.3%
Results posted
May 2019
Primary outcomePrimary: Composite Rate of Death, Myocardial Infarction (MI), and Target Vessel Revascularization (TVR) — 128; 120; 155; 99 Participants

Summary

To compile acute procedural performance and clinical outcomes data for the Promus PREMIER everolimus-eluting coronary stent system in understudied/underserved patient populations including women and minorities.

Outcome Measures

OutcomeResultp-value
PRIMARY
Composite Rate of Death, Myocardial Infarction (MI), and Target Vessel Revascularization (TVR)
128; 120; 155; 99
SECONDARY
Death
60; 35; 62; 38
SECONDARY
Myocardial Infarction (MI)
38; 17; 34; 32
SECONDARY
Target Vessel Revascularization (TVR)
58; 86; 84; 56

Eligibility Criteria

Inclusion Criteria

  • Patient must be at least 18 years of age
  • Patient must sign informed consent form
  • Patient has received at least one Promus PREMIER stent
  • Patient self-identifies as one or more of the following:
  • Female
  • Black of African Heritage
  • Hispanic/Latino
  • American Indian or Alaska native

Exclusion Criteria

  • Not applicable
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02240810). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

Back to search