search
Back to results

The Stent or Surgery (SoS) Trial

Primary Purpose

Coronary Artery Disease

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
percutaneous coronary intervention
coronary artery bypass grafting
Sponsored by
Royal Brompton & Harefield NHS Foundation Trust
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Disease focused on measuring percutaneous coronary intervention, Stent, coronary artery bypass grafting

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Written informed consent.
  • Patient has typical angina pectoris - stable or unstable symptoms.
  • Atherosclerotic coronary artery disease demonstrated with selective coronary angiography with a significant lesion present in at least two of the principal epicardial vessel systems.
  • Revascularisation procedure clinically indicated.
  • Nominated trial surgeon accepts the patient for CABG.
  • Nominated trial interventionist accepts the patient for PTCA and stent.
  • At least one identified lesion suitable and targeted for primary stent implantation.
  • A procedure for the completion of either revascularisation strategy can be performed within 6 weeks of randomisation.

Exclusion Criteria:

  • Previous CABG procedure or other thoracotomy.
  • Previous coronary interventional procedure (of any type).
  • Intervention on any cardiac valve scheduled for the index revascularisation procedure.
  • Excision or other intervention on the myocardium scheduled for the index revascularisation procedure.
  • Intervention on the great vessels, carotid arteries or aorta scheduled for the index revascularisation procedure.
  • Absent autologous graft material.
  • Non-cardiac disease influencing survival.
  • Acute myocardial infarction in the 48 hours preceding the proposed revascularisation procedure.
  • Participation in any other study that would involve deviation from the routine local management of a revascularisation procedure.
  • Allergy to anti-platelet agents in local use.
  • Language or other communication barrier.
  • Follow-up for two years not possible / Patient unreliable.

Sites / Locations

    Outcomes

    Primary Outcome Measures

    rates of repeat coronary revascularisation

    Secondary Outcome Measures

    i. Myocardial infarction free survival
    ii. Death
    iii. Myocardial infarction. (Fatal and non-fatal)
    iv. Left ventricular function as assessed by 2D echocardiography
    vi. Functional capacity - subjective by NYHA class
    vii. Anti-anginal medication requirements

    Full Information

    First Posted
    May 17, 2007
    Last Updated
    May 17, 2007
    Sponsor
    Royal Brompton & Harefield NHS Foundation Trust
    Collaborators
    Medtronic, Guidant Corporation, Schneider, British Heart Foundation
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT00475449
    Brief Title
    The Stent or Surgery (SoS) Trial
    Official Title
    A Randomised Controlled Trial to Compare Coronary Artery Bypass Grafting With Percutaneous Transluminal Coronary Angioplasty and Primary Stent Implantation in Patients With Multi-Vessel Coronary Artery Disease
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2007
    Overall Recruitment Status
    Completed
    Study Start Date
    November 1996 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    February 2006 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Royal Brompton & Harefield NHS Foundation Trust
    Collaborators
    Medtronic, Guidant Corporation, Schneider, British Heart Foundation

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    This study compared two different methods of restoring blood flow to the heart when there has been a narrowing or blockage in the blood vessels that supply the heart. Currently there are two different ways of restoring blood flow. One is heart surgery where a surgeon operates directly on the heart, through an incision in the breast bone (sternum) and takes segments of the patient's (non-essential) veins or arteries and then uses these to bypass blocked or narrowed segments in the coronary arteries. This way additional blood can be "piped" into the heart muscle wall. The second method is coronary angioplasty with stent implantation. Coronary angioplasty is a non-surgical method performed under a local anaesthetic. During angioplasty a special balloon is advanced to the site of a coronary narrowing, then inflated to make it expand and this action removes the narrowing. This is a more simple and less invasive than surgery but its value has been limited by a tendency for narrowings to reoccur(restenosis) in the six months following the treatment. When this happens a repeat procedure is often performed. To reduce the incidence of restenosis coronary stents are implanted. These are tubular metal scaffold devices that are placed inside a coronary artery at the site of a previous narrowing to help keep the artery open. These devices are usually delivered on an angioplasty balloon and expanded into place. Both treatments are equally effective at preventing death and subsequent myocardial infarction and most doctors are happy to recommend either option. Angioplasty offers a more simple initial procedure but with a chance of needing a repeat performance. Bypass surgery represents a more significant initial undertaking with a longer recovery and convalescent period but in most cases, provides good relief of symptoms. Patient preference plays an important part in the decision process. Bypass grafting is currently the therapy most frequently performed world-wide. Angioplasty has a number of important advantages but the need for repeat procedures currently limits its appeal. Since these trials were performed there have been important advances in angioplasty techniques. Prominent amongst these has been the development and use of Coronary Stents which has been shown (in clinical trials) to reduce the need for repeat procedures after an initial angioplasty. Consequently stent implantation is now in routine use world wide. If angioplasty is performed with coronary stent implantation then this may reduce the need for repeat procedures and address the principal factor currently limiting the value of this approach. If the results were found to be as good as with bypass grafting then patients could benefit from a shorter hospital stay, a less traumatic operation and a shorter recovery period. We therefore wish to compare the outcomes in patients treated with a) bypass grafting or b) angioplasty with coronary stent implantation.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Coronary Artery Disease
    Keywords
    percutaneous coronary intervention, Stent, coronary artery bypass grafting

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    988 (Actual)

    8. Arms, Groups, and Interventions

    Intervention Type
    Procedure
    Intervention Name(s)
    percutaneous coronary intervention
    Intervention Type
    Procedure
    Intervention Name(s)
    coronary artery bypass grafting
    Primary Outcome Measure Information:
    Title
    rates of repeat coronary revascularisation
    Time Frame
    median 2 years, range 1-4 years
    Secondary Outcome Measure Information:
    Title
    i. Myocardial infarction free survival
    Time Frame
    median 2 years, range 1-4 years
    Title
    ii. Death
    Time Frame
    median 2 and 6 years
    Title
    iii. Myocardial infarction. (Fatal and non-fatal)
    Time Frame
    median 2 years, range 1-4 years
    Title
    iv. Left ventricular function as assessed by 2D echocardiography
    Time Frame
    median 2 years, range 1-4 years
    Title
    vi. Functional capacity - subjective by NYHA class
    Time Frame
    median 2 years, range 1-4 years
    Title
    vii. Anti-anginal medication requirements
    Time Frame
    median 2 years, range 1-4 years

    10. Eligibility

    Sex
    All
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Written informed consent. Patient has typical angina pectoris - stable or unstable symptoms. Atherosclerotic coronary artery disease demonstrated with selective coronary angiography with a significant lesion present in at least two of the principal epicardial vessel systems. Revascularisation procedure clinically indicated. Nominated trial surgeon accepts the patient for CABG. Nominated trial interventionist accepts the patient for PTCA and stent. At least one identified lesion suitable and targeted for primary stent implantation. A procedure for the completion of either revascularisation strategy can be performed within 6 weeks of randomisation. Exclusion Criteria: Previous CABG procedure or other thoracotomy. Previous coronary interventional procedure (of any type). Intervention on any cardiac valve scheduled for the index revascularisation procedure. Excision or other intervention on the myocardium scheduled for the index revascularisation procedure. Intervention on the great vessels, carotid arteries or aorta scheduled for the index revascularisation procedure. Absent autologous graft material. Non-cardiac disease influencing survival. Acute myocardial infarction in the 48 hours preceding the proposed revascularisation procedure. Participation in any other study that would involve deviation from the routine local management of a revascularisation procedure. Allergy to anti-platelet agents in local use. Language or other communication barrier. Follow-up for two years not possible / Patient unreliable.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Rodney H Stables
    Organizational Affiliation
    Liverpool Cardiothoracic Centre
    Official's Role
    Study Chair
    First Name & Middle Initial & Last Name & Degree
    Ulrich Sigwart
    Organizational Affiliation
    University Hospital, Geneva
    Official's Role
    Study Chair
    First Name & Middle Initial & Last Name & Degree
    Spencer King
    Organizational Affiliation
    Fuqua Heart Centre of Atlanta Piedmont Hospital
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    John Pepper
    Organizational Affiliation
    Royal Brompton & Harefield NHS Foundation Trust
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Peter Wahrborg
    Organizational Affiliation
    Institute of Stress Medicine
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    William Weintraub
    Organizational Affiliation
    Christiana Centre for Outcomes Research
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Jacobus Lubsen
    Organizational Affiliation
    Erasmus Medical Centre Rotterdam
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Petros Nihoyannopolous
    Organizational Affiliation
    Hammersmith Hospitals NHS Trust
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    18606919
    Citation
    Booth J, Clayton T, Pepper J, Nugara F, Flather M, Sigwart U, Stables RH; SoS Investigators. Randomized, controlled trial of coronary artery bypass surgery versus percutaneous coronary intervention in patients with multivessel coronary artery disease: six-year follow-up from the Stent or Surgery Trial (SoS). Circulation. 2008 Jul 22;118(4):381-8. doi: 10.1161/CIRCULATIONAHA.107.739144. Epub 2008 Jul 7.
    Results Reference
    derived

    Learn more about this trial

    The Stent or Surgery (SoS) Trial

    We'll reach out to this number within 24 hrs