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The Comparative Effectiveness of Hybrid Revascularization (MIDCAB Then PCI) With DES Versus Multivessel DES PCI or CABG (HREVS)

Primary Purpose

Coronary Artery Disease, Myocardial Ischemia, Coronary Disease

Status
Completed
Phase
Not Applicable
Locations
Russian Federation
Study Type
Interventional
Intervention
Hybrid (MIDCAB+PCI)
PCI
CABG
Sponsored by
Russian Academy of Medical Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Disease focused on measuring multivessel PCI,MIDCAB,CABG, Hybrid coronary revascularization

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Multi-vessel coronary artery disease with ≥ 70% and <96% artery stenosis (according to QCA)
  2. I-IV CCS functional class of angina
  3. Asymptomatic patients with stress-test documented ischemia.
  4. Patients at 1 month after acute myocardial infarction
  5. Ability to perform either of revascularization methods (Hybrid, MVD-PCI, CABG).
  6. Consensus on the treatment strategy between the members of the working group, including cardiologist, cardiac surgeon and interventional specialist.
  7. Patients must have signed an informed consent.

Exclusion Criteria:

  1. Pregnancy.
  2. Acute coronary syndrome.
  3. Previous CABG.
  4. Previous stent thrombosis.
  5. Severe comorbidity with high procedural risk for either of the studied strategies.
  6. Severe peripheral artery disease.
  7. Other serious diseases limiting life expectancy (e.g. oncology)
  8. Inability for long-term follow-up.
  9. Participation in other clinical trials.
  10. Inability to take dual antithrombotic therapy.

Angiographic exclusion criteria

  1. Critical stenosis (>95%) in RCA,LAD, CX or Intermediate artery, feasible for revascularization.
  2. Stenosis of left main ≥ 50%.
  3. Coronary artery occlusion of the major vessel.
  4. Single vessel disease.
  5. Need for emergency revascularization (ACS).

Sites / Locations

  • Research Institute of Complex Issues of Cardiovascular Diseases

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Other

Other

Other

Arm Label

Hybrid group

PCI

CABG

Arm Description

Hybrid approach (Minimally invasive off-pump revascularization of the left anterior descending artery (LAD) with the left internal mammary artery (LIMA) bypass followed by consecutive percutaneous coronary intervention (PCI) in the rest of the arteries with drug eluting stents (DES) (Hybrid group, n=50)

Multi-vessel PCI with DES (MV-PCI group, n=50)

Coronary artery bypass graft (CABG) treatment (CABG group, n=50)

Outcomes

Primary Outcome Measures

Residual ischemia
≥5% residual ischemia by single photon emission computed tomography (SPECT)

Secondary 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.
Procedural success
Procedural success: The treatment will be considered successful when a complete hybrid revascularisation in the absence of complications during the index hospitalization has been achieved.
Procedural and post-procedural blood loss and number of transfusions
dynamics of hemoglobin at admission and discharge, the number of blood transfusions (in units), classification of bleeding BARC
Recovery time
Time Frame: from the end of the intervention up to discharge from the hospital. Total duration of hospital admission
Target vessel/graft failure
(for any of the target vessels in a given patient - stented or grafted) = a composite of cardiac death, MI attributable to the target vessel, or clinically-driven [ie, not angio-driven] Target Vessel Revascularization (TVR);
Restenosis
angiographically-detected target lesion stenosis >50% [diameter stenosis] or graft stenosis >50%;

Full Information

First Posted
October 1, 2012
Last Updated
September 27, 2017
Sponsor
Russian Academy of Medical Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT01699048
Brief Title
The Comparative Effectiveness of Hybrid Revascularization (MIDCAB Then PCI) With DES Versus Multivessel DES PCI or CABG
Acronym
HREVS
Official Title
Prospective, Single-center, Randomized Trial, Intended to Compare Three Revascularization Strategies in Patients With Multi-vessel Coronary Artery Disease
Study Type
Interventional

2. Study Status

Record Verification Date
September 2017
Overall Recruitment Status
Completed
Study Start Date
December 1, 2012 (Actual)
Primary Completion Date
March 1, 2017 (Actual)
Study Completion Date
September 16, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Russian Academy of Medical Sciences

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Minimally invasive revascularization of the left anterior descending artery followed by stent implantation versus percutaneous coronary intervention or coronary artery bypass in patients with multi-vessel coronary disease
Detailed Description
Prospective, single-center, randomized trial, intended to compare three revascularization strategies in patients with multi-vessel coronary artery disease: Hybrid approach (Minimally invasive off-pump revascularization of the left anterior descending artery (LAD) with left internal mammary artery (LIMA) bypass followed by consecutive percutaneous coronary intervention (PCI) in the rest of the arteries with drug eluting stents (DES) (Hybrid group, n=50) Multi-vessel PCI with DES (MV-PCI group, n=50) Coronary artery bypass graft (CABG) treatment (CABG group, n=50) PCI in Hybrid and MV-PCI group will be performed with the same 2nd generation clinically proven DES (Xience V, Xience Prime). Study objective Compare three different revascularization strategies in patients with multi-vessel coronary disease The endpoints: The primary endpoints: I. % ischemic myocardium on a 12-month follow-up scan with single photon emission computed tomography (SPECT); The secondary endpoints: I. Major adverse cardiac and cerebral events (MACCE), including (1) death, (2) non-fatal myocardial infarction (non-fatal MI), transitory ischemic attack (TIA) or stroke within 30 days, 12 months and 5-year follow-up; II. Target vessel/graft failure (for any of the target vessels in a given patient - stented or grafted) = a composite of cardiac death, MI attributable to the target vessel, or clinically-driven [ie, not angio-driven] Target Vessel Revascularization (TVR); III. Restenosis = angiographically-detected target lesion stenosis >50% [diameter stenosis] or graft stenosis >50%; IV. Procedural success: The treatment will be considered successful when a revascularisation in the absence of complications during the index hospitalization has been achieved; V. Procedural and post-procedural hemorrhagic complications [ Time Frame: up to discharge from the hospital ]; VI. Recovery time [ Time Frame: up to discharge from the hospital ];

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease, Myocardial Ischemia, Coronary Disease, Heart Diseases
Keywords
multivessel PCI,MIDCAB,CABG, Hybrid coronary revascularization

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Hybrid group
Arm Type
Other
Arm Description
Hybrid approach (Minimally invasive off-pump revascularization of the left anterior descending artery (LAD) with the left internal mammary artery (LIMA) bypass followed by consecutive percutaneous coronary intervention (PCI) in the rest of the arteries with drug eluting stents (DES) (Hybrid group, n=50)
Arm Title
PCI
Arm Type
Other
Arm Description
Multi-vessel PCI with DES (MV-PCI group, n=50)
Arm Title
CABG
Arm Type
Other
Arm Description
Coronary artery bypass graft (CABG) treatment (CABG group, n=50)
Intervention Type
Procedure
Intervention Name(s)
Hybrid (MIDCAB+PCI)
Other Intervention Name(s)
MIDCAB
Intervention Description
Hybrid approach (Minimally invasive of-pump revascularization of the left anterior descending artery (LAD) via left internal mammary artery (LIMA) bypass with consecutive percutaneous coronary intervention (PCI) in the rest arteries with drug eluting stents (DES). The revascularization will be performed in two stages within a 3-days interval
Intervention Type
Procedure
Intervention Name(s)
PCI
Intervention Description
Multi-vessel PCI with DES
Intervention Type
Procedure
Intervention Name(s)
CABG
Intervention Description
Coronary artery bypass graft (CABG) treatment
Primary Outcome Measure Information:
Title
Residual ischemia
Description
≥5% residual ischemia by single photon emission computed tomography (SPECT)
Time Frame
6 - to 18-month follow-up
Secondary 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 5 years
Title
Procedural success
Description
Procedural success: The treatment will be considered successful when a complete hybrid revascularisation in the absence of complications during the index hospitalization has been achieved.
Time Frame
up to discharge from the hospital
Title
Procedural and post-procedural blood loss and number of transfusions
Description
dynamics of hemoglobin at admission and discharge, the number of blood transfusions (in units), classification of bleeding BARC
Time Frame
up to discharge from the hospital
Title
Recovery time
Description
Time Frame: from the end of the intervention up to discharge from the hospital. Total duration of hospital admission
Time Frame
up to discharge from the hospital
Title
Target vessel/graft failure
Description
(for any of the target vessels in a given patient - stented or grafted) = a composite of cardiac death, MI attributable to the target vessel, or clinically-driven [ie, not angio-driven] Target Vessel Revascularization (TVR);
Time Frame
6- to 18-month follow-up
Title
Restenosis
Description
angiographically-detected target lesion stenosis >50% [diameter stenosis] or graft stenosis >50%;
Time Frame
6- to 18-month follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Multi-vessel coronary artery disease with ≥ 70% and <96% artery stenosis (according to QCA) I-IV CCS functional class of angina Asymptomatic patients with stress-test documented ischemia. Patients at 1 month after acute myocardial infarction Ability to perform either of revascularization methods (Hybrid, MVD-PCI, CABG). Consensus on the treatment strategy between the members of the working group, including cardiologist, cardiac surgeon and interventional specialist. Patients must have signed an informed consent. Exclusion Criteria: Pregnancy. Acute coronary syndrome. Previous CABG. Previous stent thrombosis. Severe comorbidity with high procedural risk for either of the studied strategies. Severe peripheral artery disease. Other serious diseases limiting life expectancy (e.g. oncology) Inability for long-term follow-up. Participation in other clinical trials. Inability to take dual antithrombotic therapy. Angiographic exclusion criteria Critical stenosis (>95%) in RCA,LAD, CX or Intermediate artery, feasible for revascularization. Stenosis of left main ≥ 50%. Coronary artery occlusion of the major vessel. Single vessel disease. Need for emergency revascularization (ACS).
Facility Information:
Facility Name
Research Institute of Complex Issues of Cardiovascular Diseases
City
Kemerovo
State/Province
Kemerovo region
ZIP/Postal Code
650002
Country
Russian Federation

12. IPD Sharing Statement

Citations:
PubMed Identifier
34016423
Citation
Ganyukov VI, Kochergin NA, Shilov AA, Tarasov RS, Skupien J, Kozyrin KA, Barbarash OL, Musialek P. Randomized Clinical Trial of Surgical Versus Percutaneous Versus Hybrid Multivessel Coronary Revascularization: 3 Years' Follow-Up. JACC Cardiovasc Interv. 2021 May 24;14(10):1163-1165. doi: 10.1016/j.jcin.2021.02.037. No abstract available.
Results Reference
derived
PubMed Identifier
31969796
Citation
Ganyukov V, Kochergin N, Shilov A, Tarasov R, Skupien J, Szot W, Kokov A, Popov V, Kozyrin K, Barbarash O, Barbarash L, Musialek P. Randomized Clinical Trial of Surgical vs. Percutaneous vs. Hybrid Revascularization in Multivessel Coronary Artery Disease: Residual Myocardial Ischemia and Clinical Outcomes at One Year-Hybrid coronary REvascularization Versus Stenting or Surgery (HREVS). J Interv Cardiol. 2020 Jan 3;2020:5458064. doi: 10.1155/2020/5458064. eCollection 2020.
Results Reference
derived

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The Comparative Effectiveness of Hybrid Revascularization (MIDCAB Then PCI) With DES Versus Multivessel DES PCI or CABG

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