CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 3,691 enrolled
Drug / intervention
PCIprocedure
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01116882
NCT01116882N/ACompleted
CompareCT.gov

A Randomized Trial to Compare Percutaneous Coronary Intervention Between Massachusetts Hospitals With Cardiac Surgery-On-Site and Community Hospitals Without Cardiac Surgery-On-Site

Baim Institute for Clinical Research·interventional·Posted May 5, 2010·Updated Apr 7, 2015

In Brief

A clinical study evaluating PCI for Coronary Artery Diseases. Completed, enrolled 3,691 participants across 17 sites.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCoronary Artery Diseases
CountriesUnited States
CollaboratorsBrockton Hospital, Good Samaritan Hospital Medical Center, New York, Norwood Hospital, Holy Family Hospital, Methuen, MA, Lawrence General Hospital, Lowell General Hospital, Melrose Wakefield Hospital, Metro West Medical Center, Saints Memorial Medical Center, South Shore Hospital

Timeline

N/ACompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMay 5, 2010
Enrollment StartJun 1, 2006
Primary CompletionJun 1, 2012
Study CompletionDec 1, 2012
TodayJul 2, 2026
Enrollment to primary: 6 yearsPosted 16.2 years ago

Interventions

PCIprocedure