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Drug-eluting-stents for Unprotected Left Main Stem Disease (ISAR-LEFT-MAIN)

Primary Purpose

Coronary Disease

Status
Completed
Phase
Phase 4
Locations
Germany
Study Type
Interventional
Intervention
Sirolimus-eluting stent
Paclitaxel-eluting stent
Sponsored by
Deutsches Herzzentrum Muenchen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Disease

Eligibility Criteria

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

Inclusion Criteria: Patients older than age 18 with ischemic symptoms or evidence of myocardial ischemia in the presence of ≥50% stenosis located in unprotected LMCA who are unable to undergo coronary artery bypass graft (CABG) Pretreatment with a loading dose of 300-600 mg clopidogrel Informed, written consent Exclusion Criteria: Cardiogenic shock; ST-segment elevation acute myocardial infarction within 48 h from symptom onset; In-stent restenosis; Malignancies or other comorbid conditions with life expectancy less than one year; Prior coronary artery bypass surgery with revascularization of left anterior descending (LAD) and/or left circumflex (LCx) coronary artery Planned staged percutaneous coronary intervention (PCI) procedure within 30 days from index procedure or prior PCI within the last 30 days Left main size >4.5mm An elective surgical procedure is planned during the first six months post enrolment; Known allergy to the study medications Pregnancy Patient's inability to fully cooperate with the study protocol

Sites / Locations

  • Deutsches Herzzentrum
  • First Medizinische Klinik, Klinikum rechts der Isar

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

A

B

Arm Description

Sirolimus-eluting stent (Cypher)

Paclitaxel-eluting stent (Taxus)

Outcomes

Primary Outcome Measures

Major adverse cardiac events (composite of death, myocardial infarction and target lesion revascularization) at one year

Secondary Outcome Measures

Angiographic restenosis at 6-9 month follow-up angiography (based on left main area analysis)

Full Information

First Posted
August 22, 2005
Last Updated
March 12, 2010
Sponsor
Deutsches Herzzentrum Muenchen
Collaborators
Technical University of Munich
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1. Study Identification

Unique Protocol Identification Number
NCT00133237
Brief Title
Drug-eluting-stents for Unprotected Left Main Stem Disease (ISAR-LEFT-MAIN)
Official Title
Prospective, Randomized Trial of the Sirolimus-Eluting Stent and Paclitaxel-Eluting Stent for the Treatment of Unprotected Left Main Coronary Artery Disease(ISAR-LEFT-MAIN)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2008
Overall Recruitment Status
Completed
Study Start Date
July 2005 (undefined)
Primary Completion Date
June 2008 (Actual)
Study Completion Date
June 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Deutsches Herzzentrum Muenchen
Collaborators
Technical University of Munich

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to evaluate the efficacy of sirolimus- and paclitaxel-eluting stents for treatment of unprotected left main coronary artery disease.
Detailed Description
With the advent of coronary stents and improvements in periprocedural antithrombotic regimen, the spectrum of indications of percutaneous coronary interventions has continuously expanded for patients with coronary heart disease, gaining ground in what have been traditionally considered as domains of coronary bypass surgery. Several groups reported the outcomes of patients with unprotected left main coronary artery (LMCA) disease treated with stenting. Most of them found that LMCA stenting was feasible and safe, and, in low-risk patients, it was associated with minimal periprocedural complications and low long-term morbidity and mortality. Despite these encouraging reports, a widespread use of this technique has been hampered by the still high incidence of restenosis. It is commonly accepted that coronary bypass graft surgery and stenting for unprotected LMCA disease are associated with similar rates of mortality, and that the higher incidence of restenosis and greater need for revascularization procedures after LMCA stenting remain the major contributors for the observed difference in clinical efficacy between both therapies. The recent introduction of stents eluting anti-restenotic drugs, with sirolimus and paclitaxel the most studied compounds, has opened new perspectives for the prevention of restenosis. Several randomized trials have reported excellent results in the reduction of restenosis and need for reinterventions with drug-eluting stents (DES). Although, none of these trials studied the benefit of DES for lesions located in the LMCA, their results suggested that use of these new devices may be particularly helpful for the reduction of restenosis in the group of patients with left main trunk disease. This is supported by the findings of several series of patients with unprotected LMCA disease who have been successfully treated with DES. Importantly, for patients who are unable to undergo CABG due to cardiac surgeons' refusal (poor surgical candidates) or their own unwillingness, stenting with DES remains the only revascularization alternative. Recent guidelines of PCI recommend stenting, preferentially with DES, for unprotected LMCA in the absence of other revascularization options. Comparison: Sirolimus-eluting stents compared with paclitaxel-eluting stent for treatment of lesions allocated at left main trunk.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
607 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Active Comparator
Arm Description
Sirolimus-eluting stent (Cypher)
Arm Title
B
Arm Type
Active Comparator
Arm Description
Paclitaxel-eluting stent (Taxus)
Intervention Type
Device
Intervention Name(s)
Sirolimus-eluting stent
Other Intervention Name(s)
Cypher
Intervention Description
cypher stent is implanted due to randomization.
Intervention Type
Device
Intervention Name(s)
Paclitaxel-eluting stent
Other Intervention Name(s)
Taxus
Intervention Description
taxus stent is implanted due to randomization.
Primary Outcome Measure Information:
Title
Major adverse cardiac events (composite of death, myocardial infarction and target lesion revascularization) at one year
Time Frame
one year
Secondary Outcome Measure Information:
Title
Angiographic restenosis at 6-9 month follow-up angiography (based on left main area analysis)
Time Frame
6-9 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients older than age 18 with ischemic symptoms or evidence of myocardial ischemia in the presence of ≥50% stenosis located in unprotected LMCA who are unable to undergo coronary artery bypass graft (CABG) Pretreatment with a loading dose of 300-600 mg clopidogrel Informed, written consent Exclusion Criteria: Cardiogenic shock; ST-segment elevation acute myocardial infarction within 48 h from symptom onset; In-stent restenosis; Malignancies or other comorbid conditions with life expectancy less than one year; Prior coronary artery bypass surgery with revascularization of left anterior descending (LAD) and/or left circumflex (LCx) coronary artery Planned staged percutaneous coronary intervention (PCI) procedure within 30 days from index procedure or prior PCI within the last 30 days Left main size >4.5mm An elective surgical procedure is planned during the first six months post enrolment; Known allergy to the study medications Pregnancy Patient's inability to fully cooperate with the study protocol
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Albert Schömig, MD
Organizational Affiliation
Deutsches Herzzentrum Muenchen
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Adnan Kastrati, MD
Organizational Affiliation
Deutsches Herzzentrum Muenchen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Deutsches Herzzentrum
City
Munich
ZIP/Postal Code
80636
Country
Germany
Facility Name
First Medizinische Klinik, Klinikum rechts der Isar
City
Munich
ZIP/Postal Code
81675
Country
Germany

12. IPD Sharing Statement

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Results Reference
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Drug-eluting-stents for Unprotected Left Main Stem Disease (ISAR-LEFT-MAIN)

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