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Percutaneous Coronary Intervention (PCI) Outcomes in Community Versus Tertiary Settings

NCT01116882 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 3691

Last updated 2015-04-07

Study results available
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Summary

The primary objective of the trial is to compare the acute safety and long term outcomes between hospitals with cardiac surgery on-site (SOS hospitals) and hospitals without cardiac surgery on-site (non-SOS hospitals) for patients with ischemic heart disease treated with elective percutaneous coronary intervention (PCI) (stable angina, acute coronary syndrome, or non-Q wave MI) presenting to non-SOS hospitals.

Conditions

  • Coronary Artery Diseases

Interventions

PROCEDURE

PCI

Sponsors & Collaborators

  • Brockton Hospital

    collaborator OTHER

  • Good Samaritan Hospital Medical Center, New York

    collaborator OTHER

  • Norwood Hospital

    collaborator OTHER

  • Holy Family Hospital, Methuen, MA

    collaborator OTHER

  • Lawrence General Hospital

    collaborator UNKNOWN

  • Lowell General Hospital

    collaborator OTHER

  • Melrose Wakefield Hospital

    collaborator UNKNOWN

  • Metro West Medical Center

    collaborator OTHER

  • Saints Memorial Medical Center

    collaborator UNKNOWN

  • South Shore Hospital

    collaborator OTHER

  • Baim Institute for Clinical Research

    lead OTHER

Principal Investigators

  • Alice K Jacobs, MD · Boston University School of Medicine , Boston Medical Center

  • Sharon-Lise Normand, Ph.D. · Harvard Medical School (HMS and HSDM)

  • Laura Mauri, M.D. · Brigham and Women's Hospital

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-06-30
Primary Completion
2012-06-30
Completion
2012-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01116882 on ClinicalTrials.gov