On Versus Off Pump Myocardial Revascularization Study (On-Off)

September 29, 2016 updated by: Medtronic Italia

ON Pump vs OFF Pump Myocardial Revascularization in High Risk Patients: a Randomized Study

Compare completeness and modality of revascularization, operative and postoperative results and 1 year clinical outcomes in unselected high risk patients referred for primary coronary artery bypass surgery. Patients will be randomized to undergo off-pump coronary artery bypass graft (OPCAB) or coronary artery bypass graft with cardiopulmonary bypass (CPB/CAB).

Study Overview

Detailed Description

The initial application of off-pump coronary artery bypass in the early nineties was mainly directed to highly selected and relatively low risk surgical patients. Since then there has been a growing body of evidence suggesting many potential advantages of the OPCAB technique over the conventional cardiopulmonary bypass (CPB) technique in different groups of high-risk patients.

On-off study is a multicentre, prospective, randomized, parallel, trial.Patients indicated for elective or urgent isolated coronary artery bypass graft with additive European System for Cardiac Operative Risk Evaluation ≥ 6 were enrolled. Patients in cardiogenic shock were excluded. Patients were randomly assigned either to coronary artery bypass surgery with cardiopulmonary bypass (ON arm) or to off-pump coronary artery bypass graft (OFF arm). The composite primary end point included operative mortality, myocardial infarction, stroke, renal failure, re-operation for bleeding and adult respiratory distress syndrome, within 30 days after surgery. The total planned sample size was 693 patients; the actual number of enrolled patients was 411,according to the results of the interim analysis scheduled at 400 enrollments (alfa-spending=0.029, Pocock method).

Study Type

Interventional

Enrollment (Actual)

411

Phase

  • Phase 4

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Bari, Italy
        • Policlinico
      • Caserta, Italy
        • S. Anna e S. Sebastiano
      • Milano, Italy, 20100
        • Ospedale Luigi Sacco
      • Roma, Italy
        • European Hospital
      • Roma, Italy
        • Ospedale S. Camillo
      • Salerno, Italy
        • Ospedale S. Giovanni di Dio e Ruggi d'Aragona
      • Torino, Italy
        • Ospedale Molinette
      • Zurich, Switzerland
        • University Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Pts candidate to a myocardial revascularization for any patter of coronary artery disease, ventricular dysfunction or any other co-morbidity
  • EUROSCORE ≥ 6
  • Pts who signed the Informed Consent
  • Age ≥ 18 years

Exclusion Criteria:

  • Patients in cardiogenic shock requiring emergency surgery or preoperative intra-aortic balloon pump
  • Patients requiring additional surgical procedures
  • Porcelain Aorta
  • Lack of informed consent

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Off-pump bypass surgery
Off-pump coronary artery bypass graft (OPCAB) using mandatory a stabilization device and advisable, but not mandatory, a heart positioner
is a method of performing a coronary bypass operation for the purpose of treating advanced coronary heart disease while the heart is still beating normally.
Active Comparator: On-pump bypass surgery
coronary artery bypass graft with cardiopulmonary bypass (CPB/CAB)
is a technique that temporarily takes over the function of the heart and lungs during surgery, maintaining the circulation of blood and the oxygen content of the body.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of Patients With Post-operative Combined Endpoint (i.e. With One or More of the Following)
Time Frame: 30 days

Number of patients with one or more of the following:

  • Operative Mortality
  • Myocardial Infarction
  • Postoperative neurological complications
  • Renal failure
  • ARDS (Acute Respiratory Distress Syndrome)
  • Bleeding
30 days

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of Patients With Secondary Combined Endpoint (i.e. With One or More of the Following)
Time Frame: 30 days

Number of patients with one of more of the following:

  • Post-operative Atrial Fibrillation
  • IAPB (Intra-Aortic Balloon Pump) insertion and low cardiac output syndrome
  • Ventilation > 24h
  • Sternal wound infection or dehiscence
30 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Massimo Lemma, Dr., Ospedale Sacco-Milano

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

September 1, 2006

Primary Completion (Actual)

June 1, 2010

Study Completion (Actual)

June 1, 2011

Study Registration Dates

First Submitted

February 4, 2011

First Submitted That Met QC Criteria

February 4, 2011

First Posted (Estimate)

February 7, 2011

Study Record Updates

Last Update Posted (Estimate)

November 21, 2016

Last Update Submitted That Met QC Criteria

September 29, 2016

Last Verified

September 1, 2016

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

IPD Plan Description

The main manuscript with the results of the primary endpoint analysis was published in December 2011.There are no plans to make individual partecipant data available

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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