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Comparative Effectiveness of the Minimally Invasive Coronary Artery Bypass Grafting

Primary Purpose

Coronary Artery Disease, Myocardial Ischemia, Heart Diseases

Status
Unknown status
Phase
Not Applicable
Locations
Belarus
Study Type
Interventional
Intervention
MICS CABG
OPCABG
ONCABG
Octopus® Nuvo, Starfish® Non-Sternotomy, thoracic retractor (ThoraTrak®)
Starfish®, Octopus®, Clearview® blower, ClearView® Shunt
Sponsored by
Vitebsk Regional Clinical Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Disease focused on measuring MICS CABG OPCABG ONCABG CAD

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Multi-vessel coronary artery disease with ≥ 70% artery stenosis (according to QCA)
  • II-IV Canadian Cardiovascular Society functional class of angina
  • Patients at 1 month after acute myocardial infarction
  • Ability to perform either of revascularization methods (MICS CABG, OPCABG, ONCABG)
  • Patients must have signed an informed consent

Exclusion Criteria:

  • Pregnancy.
  • Acute coronary syndrome.
  • Previous CABG.
  • Severe comorbidity with high procedural risk for either of the studied strategies.
  • Mental diseases which block the revascularization procedure.
  • Severe peripheral artery disease.
  • Other serious diseases limiting life expectancy (e.g. oncology)
  • Inability for long-term follow-up.
  • Participation in other clinical trials.
  • Single vessel disease.
  • Need for emergency revascularization (Acute MI, Acute coronary syndrome etc.)

Sites / Locations

  • Vitebsk regional clinical hospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Active Comparator

Arm Label

MICS CABG

OPCABG

ONCABG

Arm Description

Minimally invasive cardiac surgery coronary artery bypass grafting (complete multivessel minimally invasive off-pump revascularization via left minithoracotomy), which is performed with a help of Octopus® Nuvo, Starfish® Non-Sternotomy, ThoraTrak®, Starfish®, Octopus®, Clearview® blower, ClearView® Shunt. (MICS CABG group, n=50)

Off-pump coronary artery bypass grafting treatment which is performed with a help of Starfish®, Octopus®, Clearview® blower, ClearView® Shunt. (OPCABG group, n=50)

On-pump coronary artery bypass grafting treatment (ONCABG group, n=50)

Outcomes

Primary Outcome Measures

MACCE
Major adverse cardiac and cerebral events (MACCE), including death, a composite of major cardiac and cerebrovascular events, i.e. the first occurrence of any of the following events: Death from any cause. From cardiovascular causes. From noncardiovascular causes. Stroke or transitory ischemic attack (TIA) MI Hospitalization for repeat revascularization procedure, target (vessel) revascularization by means of PCI or CABG.

Secondary Outcome Measures

Procedural success
Procedural success: The MICS CABG treatment will be considered successful when a complete or functionally reasonable revascularisation in the absence of complications during the index hospitalization has been achieved.
Transfusion rate
Proportion of patients who received at least one transfusion of any blood product
Recovery time
Length of postoperative hospital stay from the end of the intervention up to discharge from the hospital
New York Heart Association (NYHA) class modification with respect to baseline
Wound infection
Drainage of purulent material from the wound (superficial or deep)
New-onset renal failure
The need for temporary or permanent renal dialysis of any type
Respiratory insufficiency
Cumulative requirement for intubation and ventilation of 72 h or more, at any time during the postoperative stay
Return to full physical activity postoperatively
(1) the ability to walk 30 min or more per day and (2) the ability to use the upper torso and arms without restriction for activities of daily living
Intensive care unit (ICU) stay

Full Information

First Posted
January 19, 2014
Last Updated
December 19, 2015
Sponsor
Vitebsk Regional Clinical Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02047266
Brief Title
Comparative Effectiveness of the Minimally Invasive Coronary Artery Bypass Grafting
Official Title
Comparative Effectiveness of the Minimally Invasive Coronary Artery Bypass Grafting (MICS CABG) Versus Off Pump (OPCABG) and on Pump Coronary Artery Bypass Grafting (ONCABG) in Patients With Multi-vessel Coronary Disease
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Unknown status
Study Start Date
January 2014 (undefined)
Primary Completion Date
June 2016 (Anticipated)
Study Completion Date
June 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Vitebsk Regional Clinical Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to compare three different revascularization strategies in patients with multi-vessel coronary disease: MICS CABG, OPCABG and ONCABG. The study hypothesis: MICS CABG (Minimally invasive cardiac surgery coronary artery bypass grafting) has advantages in comparison with conventional off-pump (OPCABG) and on-pump coronary artery bypass grafting (ONCABG) concerning major adverse cardiac and cerebral events (MACCE) and procedural success.
Detailed Description
Prospective, single-center, randomized trial, intended to compare three different revascularization strategies in patients with multi-vessel coronary artery disease: MICS CABG. Minimally invasive cardiac surgery coronary artery bypass grafting (complete multivessel minimally invasive off-pump revascularization via left minithoracotomy). (MICS CABG group, n=50). OPCABG. Off-pump coronary artery bypass grafting treatment (OPCABG group, n=50). ONCABG. On-pump coronary artery bypass grafting treatment (ONCABG group, n=50). The endpoints: The primary endpoints will be death, MI, stroke, or new myocardial ischemia and will be target vessel revascularization and non-target vessel revascularization at 30 days, 12 months and 3-year follow-up. The secondary endpoints: Procedural success, Procedural and post-procedural blood loss and number of transfusions, Wound complications, Recovery time, Heart Failure (New York Heart Association (NYHA)), Life quality assessed by one of the life quality questionnaires.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease, Myocardial Ischemia, Heart Diseases
Keywords
MICS CABG OPCABG ONCABG CAD

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
MICS CABG
Arm Type
Experimental
Arm Description
Minimally invasive cardiac surgery coronary artery bypass grafting (complete multivessel minimally invasive off-pump revascularization via left minithoracotomy), which is performed with a help of Octopus® Nuvo, Starfish® Non-Sternotomy, ThoraTrak®, Starfish®, Octopus®, Clearview® blower, ClearView® Shunt. (MICS CABG group, n=50)
Arm Title
OPCABG
Arm Type
Active Comparator
Arm Description
Off-pump coronary artery bypass grafting treatment which is performed with a help of Starfish®, Octopus®, Clearview® blower, ClearView® Shunt. (OPCABG group, n=50)
Arm Title
ONCABG
Arm Type
Active Comparator
Arm Description
On-pump coronary artery bypass grafting treatment (ONCABG group, n=50)
Intervention Type
Procedure
Intervention Name(s)
MICS CABG
Intervention Description
Minimally invasive coronary artery bypass grafting - beating heart multi-vessel procedure in which the anastomoses are performed under direct vision through a lateral left mini-thoracotomy. The left internal thoracic artery is used to graft the left anterior descending artery or circumflex artery territories. Radial artery or saphenous vein are used (Y - grafts) to graft another myocardial territories. Right internal thoracic artery can be used as free Y-graft, as in-situ graft with radial artery (extension technique) or as in-situ graft without composite technique. Right gastroepiploic artery can be used to graft right coronary artery territory. Hybrid approach (MICS CABG + PCI), parallel transfemoral extracorporeal circulation without cardioplegia and CABG from the ascending aorta are acceptable for achievement of the complete revascularization.
Intervention Type
Procedure
Intervention Name(s)
OPCABG
Intervention Description
Off-pump coronary artery bypass grafting via sternotomy (aortocoronary bypass grafting or aortic no-touch technique composite grafting). Mechanical Devices are used for coronary artery stabilization and heart positioning. Pericardial traction sutures are used to position the heart where appropriate. Blowers and Intracoronary shunts are used routinely. Anticoagulation is obtained using sodium heparin at a dose of 2mg/kg with supplemental doses to maintain adequate heparinisation (Activated clotting time>250seconds).
Intervention Type
Procedure
Intervention Name(s)
ONCABG
Intervention Description
On-pump coronary artery bypass grafting via sternotomy (aortocoronary bypass grafting or aortic no-touch technique composite grafting). Normothermic cardiopulmonary bypass and complex blood ante-retrograde cardioplegia are used. All patients are cannulated with an proximal aortic cannula and two-stage right atrial cannula. Extracorporeal circulation is provided by the Terumo System-1 heart-lung machine using cardiopulmonary bypass systems with physiological surfaces and opened venous reservoirs. The left internal thoracic artery is used to graft the left anterior descending artery, and radial artery or saphenous vein segments are used to graft another myocardial territories. Anticoagulation is obtained using sodium heparin at a dose of 3mg/kg (ACT, activated clotting time>450seconds).
Intervention Type
Device
Intervention Name(s)
Octopus® Nuvo, Starfish® Non-Sternotomy, thoracic retractor (ThoraTrak®)
Intervention Description
Octopus® Nuvo - MICS CABG tissue stabilizer available for minimally invasive procedures. It minimizes the motion of a small area of the heart while the rest of the heart continues to beat normally and allows to perform anastomosis through a small incision. Starfish® Non-Sternotomy (NS) - MICS CABG heart positioner available for minimally invasive procedures. It allows for the positioning of the beating heart through a small incision, bringing coronary targets into the operative thoracotomy window. ThoraTrak® - a reusable, stainless steel MICS thoracic retractor system for minimally invasive heart surgery with multiple interchangeable blades, which allows to harvest left internal thoracic artery and to perform anastomosis through a small left thoracotomy(Medtronic, Inc., Minneapolis, MN).
Intervention Type
Device
Intervention Name(s)
Starfish®, Octopus®, Clearview® blower, ClearView® Shunt
Intervention Description
Starfish® - heart positioner is designed to position and to hold the heart to give the surgeon easy access to the vessel requiring the bypass graft. Octopus® - tissue stabilizer minimizes / limits the motion of a small area of the heart while the rest of the heart continues to beat normally. This allows the surgeon to perform CABG surgery without stopping of the heart and without using the heart-lung machine. ClearView® Blower is designed to improve visualization of the surgical site. An irrigation mist gently clears blood from the site, improving visualization without drying or desiccating delicate tissue. The ClearView® shunt - Intracoronary shunt provides a clear anastomotic site during the procedure while providing blood flow to the distal myocardium (Medtronic, Inc., Minneapolis, MN)
Primary Outcome Measure Information:
Title
MACCE
Description
Major adverse cardiac and cerebral events (MACCE), including death, a composite of major cardiac and cerebrovascular events, i.e. the first occurrence of any of the following events: Death from any cause. From cardiovascular causes. From noncardiovascular causes. Stroke or transitory ischemic attack (TIA) MI Hospitalization for repeat revascularization procedure, target (vessel) revascularization by means of PCI or CABG.
Time Frame
up to 3 years
Secondary Outcome Measure Information:
Title
Procedural success
Description
Procedural success: The MICS CABG treatment will be considered successful when a complete or functionally reasonable revascularisation in the absence of complications during the index hospitalization has been achieved.
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 2 weeks
Title
Transfusion rate
Description
Proportion of patients who received at least one transfusion of any blood product
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 2 weeks
Title
Recovery time
Description
Length of postoperative hospital stay from the end of the intervention up to discharge from the hospital
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 2 weeks
Title
New York Heart Association (NYHA) class modification with respect to baseline
Time Frame
up to 3 years
Title
Wound infection
Description
Drainage of purulent material from the wound (superficial or deep)
Time Frame
up to 12 months postoperatively
Title
New-onset renal failure
Description
The need for temporary or permanent renal dialysis of any type
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 2 weeks
Title
Respiratory insufficiency
Description
Cumulative requirement for intubation and ventilation of 72 h or more, at any time during the postoperative stay
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 2 weeks
Title
Return to full physical activity postoperatively
Description
(1) the ability to walk 30 min or more per day and (2) the ability to use the upper torso and arms without restriction for activities of daily living
Time Frame
up to 3 years
Title
Intensive care unit (ICU) stay
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 2 weeks
Other Pre-specified Outcome Measures:
Title
Procedural and post-procedural blood loss
Description
blood loss during operation and first twenty-four hours postoperatively
Time Frame
up to first twenty-four hours postoperatively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Multi-vessel coronary artery disease with ≥ 70% artery stenosis (according to QCA) II-IV Canadian Cardiovascular Society functional class of angina Patients at 1 month after acute myocardial infarction Ability to perform either of revascularization methods (MICS CABG, OPCABG, ONCABG) Patients must have signed an informed consent Exclusion Criteria: Pregnancy. Acute coronary syndrome. Previous CABG. Severe comorbidity with high procedural risk for either of the studied strategies. Mental diseases which block the revascularization procedure. Severe peripheral artery disease. Other serious diseases limiting life expectancy (e.g. oncology) Inability for long-term follow-up. Participation in other clinical trials. Single vessel disease. Need for emergency revascularization (Acute MI, Acute coronary syndrome etc.)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Aliaksandr A Ziankou, MD, PhD
Phone
+375297106526
Email
Zenkov_Al@rambler.ru
First Name & Middle Initial & Last Name or Official Title & Degree
Mikalai G Laiko, MD
Phone
+375333050458
Email
Nikolay99@mail.ru
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Aliaksandr A Ziankou, MD, PhD
Organizational Affiliation
Vitebsk Regional Clinical Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vitebsk regional clinical hospital
City
Vitebsk
State/Province
Vitebsk region
ZIP/Postal Code
210037
Country
Belarus
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Aliaksandr A Ziankou, MD, PhD
First Name & Middle Initial & Last Name & Degree
Mikalai G Laiko, MD
Phone
+375333050458
Email
Nikolay99@mail.ru
First Name & Middle Initial & Last Name & Degree
Aliaksandr A Ziankou, MD, PhD
First Name & Middle Initial & Last Name & Degree
Mikalai G Laiko, MD

12. IPD Sharing Statement

Learn more about this trial

Comparative Effectiveness of the Minimally Invasive Coronary Artery Bypass Grafting

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