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Nordic-Baltic Coronary Revascularization Study in Patients With Proximal Left Descending Coronary Artery (LAD) Lesion. (NOBLE-LAD)

Primary Purpose

Coronary Artery Disease

Status
Terminated
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Coronary artery bypass grafting (CABG)
Percutaneous coronary intervention (PCI)
Sponsored by
Aalborg University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Disease focused on measuring Coronary revascularization

Eligibility Criteria

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

Inclusion Criteria:

Heart Team decision on treatment

1-VD patients with stable coronary artery disease or stabilized unstable angina pectoris/NSTEMI or silent ischemia Proximal LAD (pLAD) stenosis (>90% by visual assessment or FFR <80% The lesion may be treated by both PCI and surgery

Exclusion Criteria:

ST-elevation myocardial infarction within 24 hours. Expected survival <1 year, because of high age or severe cardiac or non-cardiac disease.

Significant LM disease. Earlier CABG. PCI within 3 months. Significant valvular heart disease. Renal failure on dialysis Earlier disabling stroke Relative or absolute contraindication to dual antiplatelet therapy. Allergy relevant to the study treatments. Age < 18 years. Study required information and consent suboptimal or impossible.

Sites / Locations

  • Aalborg University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Percutaneous coronary intervention (PCI)

Coronary artery bypass grafting (CABG)

Arm Description

Currently, percutaneous coronary intervention (PCI) using balloon and drug eluting stents is the treatment of choice for treatment of a proximal LAD lesion.

Coronary artery bypass grafting is a well established treatment with documented excellent long-term results for the treatment of proximal LAD lesion.

Outcomes

Primary Outcome Measures

All-cause mortality
Death of any cause
Quality of life
By SF 12 and Seatle Angina Questionaire
MACCE
Major cardiac and cerebral adverse events (myocardial infarction, stroke, revascularization, death)

Secondary Outcome Measures

All-cause death
Death of any cause
Cardiac death
Death of cardiac disease
Spontaneous myocardial infarction
Type 1 myocardial infarction
Procedure related myocardial infarction
Myocardial infarction related to PCI or CABG
Major stroke, minor stroke and al stroke
Stroke by VARC definition
Angina
CCS angina class
Heart failure
NYHA class
Stent thrombosis
ARC-define stent thrombosis

Full Information

First Posted
May 16, 2018
Last Updated
April 5, 2021
Sponsor
Aalborg University Hospital
Collaborators
Oulu University Hospital, Region Örebro County, Pauls Stradins Clinical University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03538886
Brief Title
Nordic-Baltic Coronary Revascularization Study in Patients With Proximal Left Descending Coronary Artery (LAD) Lesion.
Acronym
NOBLE-LAD
Official Title
The Nordic-Baltic Heart Team Initiative for Improved Long-term Coronary Artery Revascularization Outcome in Patients With Proximal Left Descending Coronary Artery (LAD) Lesion. NOBLE LAD
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Terminated
Why Stopped
Impossible to involve a sufficient number of centers in the study.
Study Start Date
June 1, 2018 (Actual)
Primary Completion Date
July 31, 2019 (Actual)
Study Completion Date
July 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Aalborg University Hospital
Collaborators
Oulu University Hospital, Region Örebro County, Pauls Stradins Clinical University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The Nordic-Baltic Heart Team Initiative for improved long-term coronary artery revascularization outcome compares quality of life and survival after coronary bypass grafting (CABG) vs. percutaneous coronary intervention (PCI) in patients with 1-vessel disease and proximal stenosis of the anterior descending artery (LAD/in patients with isolated proximal left descending coronary artery (LAD) lesion
Detailed Description
It is not clear how operable 1-VD patients with stable or stabilized coronary artery disease involving a pLAD lesion should be treated to optimize long-term survival and quality of life. According to recent European guidelines, significant pLAD disease may be treated by PCI or by CABG. This recommendation is based on two meta-analyses including 1.210 and 1.952 randomized and non-randomized patients. Generally, the patients were followed for 4-5 years. The analyses reported similar rates of mortality, MI and stroke, but more repeat revascularizations after PCI. Only one study including129 patients provided more than 5-year follow-up. Thus, the there is limited documentation for long-term effect of PCI vs. surgical re-vascularization in pLAD disease. The American 2014 Guidelines on coronary revascularization recommends CABG for improved survival in patients with solitary proximal LAD stenosis. CABG The angiographic 90% LIMA patency rate after 1, 2 and 3 decades is well described and suggestive of a survival benefit of surgical revascularization. Therefore, there is scientific background for an CABG LIMA-to-LAD vs. PCI comparison in 1-VD patients with a pLAD lesion. Substantiated expectations: PCI is superior to bypass operation concerning short-term quality of life. Off-pump LIMA-to-LAD is superior to PCI concerning long-term all-cause mortality. Long-term (≥10-year) follow-up is essential to evaluate coronary revascularization strategies. Outcome may be dependent on lesion complexity, diabetes and gender.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease
Keywords
Coronary revascularization

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
1:1 randomized clinical trial
Masking
Outcomes Assessor
Masking Description
The clinical outcomes will be assessed by an independent event committee with no knowledge of treatment allocation.
Allocation
Randomized
Enrollment
4 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Percutaneous coronary intervention (PCI)
Arm Type
Active Comparator
Arm Description
Currently, percutaneous coronary intervention (PCI) using balloon and drug eluting stents is the treatment of choice for treatment of a proximal LAD lesion.
Arm Title
Coronary artery bypass grafting (CABG)
Arm Type
Experimental
Arm Description
Coronary artery bypass grafting is a well established treatment with documented excellent long-term results for the treatment of proximal LAD lesion.
Intervention Type
Procedure
Intervention Name(s)
Coronary artery bypass grafting (CABG)
Intervention Description
Revascularization of LAD lesion by CABG
Intervention Type
Procedure
Intervention Name(s)
Percutaneous coronary intervention (PCI)
Intervention Description
Revascularization of LAD lesion by PCI
Primary Outcome Measure Information:
Title
All-cause mortality
Description
Death of any cause
Time Frame
10 years
Title
Quality of life
Description
By SF 12 and Seatle Angina Questionaire
Time Frame
1 year
Title
MACCE
Description
Major cardiac and cerebral adverse events (myocardial infarction, stroke, revascularization, death)
Time Frame
1 year
Secondary Outcome Measure Information:
Title
All-cause death
Description
Death of any cause
Time Frame
1, 2, 3, 5 and 10 years
Title
Cardiac death
Description
Death of cardiac disease
Time Frame
1, 2, 3, 5 and 10 years
Title
Spontaneous myocardial infarction
Description
Type 1 myocardial infarction
Time Frame
1, 2, 3, 5 and 10 years
Title
Procedure related myocardial infarction
Description
Myocardial infarction related to PCI or CABG
Time Frame
1, 2, 3, 5 and 10 years
Title
Major stroke, minor stroke and al stroke
Description
Stroke by VARC definition
Time Frame
1, 2, 3, 5 and 10 years
Title
Angina
Description
CCS angina class
Time Frame
1, 2, 3, 5 and 10 years
Title
Heart failure
Description
NYHA class
Time Frame
1, 2, 3, 5 and 10 years
Title
Stent thrombosis
Description
ARC-define stent thrombosis
Time Frame
1, 2, 3, 5 and 10 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Heart Team decision on treatment 1-VD patients with stable coronary artery disease or stabilized unstable angina pectoris/NSTEMI or silent ischemia Proximal LAD (pLAD) stenosis (>90% by visual assessment or FFR <80% The lesion may be treated by both PCI and surgery Exclusion Criteria: ST-elevation myocardial infarction within 24 hours. Expected survival <1 year, because of high age or severe cardiac or non-cardiac disease. Significant LM disease. Earlier CABG. PCI within 3 months. Significant valvular heart disease. Renal failure on dialysis Earlier disabling stroke Relative or absolute contraindication to dual antiplatelet therapy. Allergy relevant to the study treatments. Age < 18 years. Study required information and consent suboptimal or impossible.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Leif Thuesen, MD
Organizational Affiliation
Department of Cardiology, Aalborg University Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jan Jesper Andreasen, Prof
Organizational Affiliation
Department of Cardiothoracic Surgery, Aalborg University Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Peter Sogaard, Prof
Organizational Affiliation
Department of Cardiology, aaalborg University Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Aalborg University Hospital
City
Aalborg
ZIP/Postal Code
9100
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
After publication of the trial, data will be made available for metaanalyses on request, and after accept by the steering committee.
IPD Sharing Time Frame
Study protocol and statistical analysis plan available by now.
IPD Sharing Access Criteria
At clinicaltrial.gov

Learn more about this trial

Nordic-Baltic Coronary Revascularization Study in Patients With Proximal Left Descending Coronary Artery (LAD) Lesion.

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