Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02240810 · ClinicalTrials.gov registry record

PLATINUM Diversity

A clinical trial of Coronary Artery Disease and Atherosclerosis, sponsored by Boston Scientific Corporation.

Completed
Registry status
1,501
Enrollment target
20
Study locations

NCT02240810: Completed study of Coronary Artery Disease and Atherosclerosis, sponsored by Boston Scientific Corporation.

NCT02240810 is a study of Coronary Artery Disease and Atherosclerosis that has completed, run by Boston Scientific Corporation. The registered enrollment target is 1,501 participants, above the 1,280-participant average among 219 other Coronary Artery Disease trials with a reported enrollment target (17% higher). The trial reports 20 study locations across 7 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02240810, a study of Coronary Artery Disease and Atherosclerosis, has completed, sponsored by Boston Scientific Corporation.

COMPLETED
Registry status
1,501 participants
Enrollment target
20
Study locations

Study 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.

Primary Outcome

A Clinical Events Committee (CEC), independent group of physician experts was used to evaluate all reported cases of death, MI, TVR to determine whether they met the specific protocol definition of the event. It is the CEC adjudicated result that is used in the endpoint analysis. Results for the PROMUS Element Plus study are reported in record NCT01589978

Interventions

  • DEVICE Percutaneous coronary intervention (Promus PREMIER)

Study Locations (20)

Florida

  • Bay Area Cardiology - Brandon
  • Research Physicians Network Alliance - Hollywood
  • Memorial Hospital Jacksonville - Jacksonville
  • Cardiovascular Institute of Northwest Florida - Panama City
  • Charlotte Heart & Vascular - Port Charlotte
  • Tallahassee Memorial Hospital - Tallahassee
  • Pepin Heart Hospital and Dr. Kiran C. Patel Research Institute - Tampa

California

  • Central Cardiology Medical Clinic - Bakersfield
  • Sharp Chula Vista Medical Center - Chula Vista
  • Cardiovascular Consultants Heart Center - Fresno
  • UCLA Medical Center - Los Angeles
  • Mercy General Hospital - Sacramento

Georgia

  • Emory University - Atlanta
  • University Hospital - Augusta
  • Redmond Regional Medical Center - Rome

Arkansas

  • St Bernards Heart and Vascular - Jonesboro
  • Arkansas Cardiology/Baptist Health Medical Center - Little Rock

Arizona

  • St Luke's Medical Center - Phoenix

District of Columbia

  • Capital Research Institute - Washington D.C.

Illinois

  • University of Chicago Medical Center - Chicago

Trial Details

FieldValue
Enrollment Target 1,501 participants
Start Date 2014-10
Est. Completion 2016-12
Boston Scientific Corporation

280 total trials

What the finished NCT02240810 record still lists

NCT02240810 is an observational study that tracks outcomes without assigning an intervention. Its 1,501 participants enrollment target places it among the larger protocols in the corpus, above the 1,280-participant average among 219 other Coronary Artery Disease trials with a reported enrollment target (17% higher).

The record links to 2 conditions, with Coronary Artery Disease appearing as the primary indexed condition, and to 1 intervention - of which Percutaneous coronary intervention (Promus PREMIER) is the first listed.

NCT02240810 names 20 study sites across 7 states, led by Florida, California, Georgia.

Frequently Asked Questions

What is clinical trial NCT02240810 about?

NCT02240810 is a clinical study titled "PLATINUM Diversity". 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.

What is the current status of trial NCT02240810?

This trial is currently completed. The enrollment target is 1,501 participants. The study started on 2014-10. Estimated completion is 2016-12.

What conditions does trial NCT02240810 study?

This clinical trial studies the following conditions: Coronary Artery Disease, Atherosclerosis.

What interventions are being tested in trial NCT02240810?

The interventions under investigation include: Percutaneous coronary intervention (Promus PREMIER) (DEVICE).

Who is sponsoring clinical trial NCT02240810?

This trial is sponsored by Boston Scientific Corporation, which has 280 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02240810 being conducted?

This trial has 20 study locations across Arizona, Arkansas, California, District of Columbia, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Coronary Artery Disease

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02240810's enrollment target sits among peer trials

1,501 36th of 219 higher than 184 of 219 other Coronary Artery Disease trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Coronary Artery Disease trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00178724 · 1,500 participants

    Spinal Cord Injury Registry - North American Clinical Trials Network

  • NCT00951366 · 1,500 participants

    Preterm Lung Patient Registry

  • NCT01050504 · 1,500 participants

    Collecting and Studying Blood and Tissue Samples From Patients With Locally Recurrent or Metastatic Prostate or Bladder/Urothelial Cancer

  • NCT02071134 · 1,500 participants

    Registry of Deep Brain Stimulation With the VERCISE™ System: Vercise DBS Registry

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02240810, the US trial registry maintained by the National Library of Medicine. NCT02240810 (large enrollment · wide site footprint · completed) retrieved and formatted by PlainTrial, see methodology.