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A Comparison of an Ultrathin Strut Biodegradable Polymer Sirolimus-Eluting Stent With a Durable Polymer Everolimus-Eluting Stent for Patients With Acute ST-Segment Elevation Myocardial Infarction Undergoing Primary Percutaneous Coronary Intervention (BIOSTEMI)

Primary Purpose

Coronary Artery Disease, Acute Coronary Syndrome

Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Orsiro
Xience
Sponsored by
Insel Gruppe AG, University Hospital Bern
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Disease focused on measuring Percutaneous Coronary Intervention, Stents, Drug-Eluting Stents, Coronary Artery Disease, Acute Coronary Syndrome

Eligibility Criteria

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

Inclusion Criteria:

  • Age ≥18 years
  • ST-segment elevation acute myocardial infarction
  • Primary PCI occurring within 24 hours of symptom onset
  • Presence of ≥1 acute infarct artery target vessel with one or more coronary artery stenoses in a native coronary artery from 2.25 to 4.0 mm in diameter that can be covered with one or multiple coronary stents

Exclusion Criteria

  • Known allergy to aspirin, Ticagrelor, Prasugrel, Clopidogrel, Sirolimus, Everolimus or contrast media
  • Planned surgery within 6 months of primary PCI, unless dual antiplatelet therapy could be maintained throughout the peri-surgical period
  • Currently participating in another trial before reaching the primary endpoint
  • Inability to provide informed consent
  • Non-cardiac comorbid conditions with life expectancy of less than 1 year
  • Mechanical complication of acute myocardial infarction
  • Acute myocardial infarction due to stent thrombosis

Sites / Locations

  • Kantonsspital Aarau
  • Universitätsspital Basel
  • Bern University Hospital, Dep. of Cardiology
  • Universität Freiburg
  • HUG
  • Lausanne University Hospital
  • Kantonsspital Luzern
  • Spital Wallis
  • Kantonsspital St. Gallen
  • Triemli

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Orsiro

Xience

Arm Description

Novel biodegradable-polymer sirolimus-eluting stent Orsiro

Durable-polymer everolimus-eluting stent Xience

Outcomes

Primary Outcome Measures

Number of patients with target lesion failure (TLF), a composite of cardiac death, target vessel myocardial infarction (Q-wave and non-Q-wave), or clinically driven target lesion revascularization

Secondary Outcome Measures

Number of patients with clinically indicated and not clinically indicated target lesion revascularization (TLR)
Number of patients with clinically indicated and not clinically indicated target vessel revascularization (TVR)
Number of patients with target vessel failure (TVF)
Number of patients with cardiac death
Number of patients with all-cause death (cardiac and non-cardiac)
Number of patients with myocardial infarction (Q-wave and non-Q-wave)
Number of patients with definite stent thrombosis

Full Information

First Posted
October 16, 2015
Last Updated
September 1, 2020
Sponsor
Insel Gruppe AG, University Hospital Bern
Collaborators
University of Lausanne Hospitals
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1. Study Identification

Unique Protocol Identification Number
NCT02579031
Brief Title
A Comparison of an Ultrathin Strut Biodegradable Polymer Sirolimus-Eluting Stent With a Durable Polymer Everolimus-Eluting Stent for Patients With Acute ST-Segment Elevation Myocardial Infarction Undergoing Primary Percutaneous Coronary Intervention
Acronym
BIOSTEMI
Official Title
A Comparison of an Ultrathin Strut Biodegradable Polymer Sirolimus-Eluting Stent With a Durable Polymer Everolimus-Eluting Stent for Patients With Acute ST-Segment Elevation Myocardial Infarction Undergoing Primary Percutaneous Coronary Intervention
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
April 2016 (Actual)
Primary Completion Date
April 2019 (Actual)
Study Completion Date
May 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Insel Gruppe AG, University Hospital Bern
Collaborators
University of Lausanne Hospitals

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
PCI is considered as the reperfusion strategy of choice for patients with acute STEMI. Data from RCTs and meta-analyses demonstrate a consistent and strong signal towards a significant reduction in MACE among patients with STEMI undergoing primary PCI with newer generation stents with enhanced biocompatibility. The present trial aims at filling the current gap of evidence by providing randomized data to establish the superior clinical outcome with an ultrathin strut third-generation DES with biodegradable polymer designed to improve vascular healing in patients with STEMI undergoing primary PCI, compared to the current state-of-the art second-generation DES with permanent polymer.
Detailed Description
Background Primary percutaneous coronary intervention (PCI) is considered nowadays as the reperfusion strategy of choice for patients with acute ST-segment elevation myocardial infarction (STEMI, owing to a lower risk of myocardial re-infarction and improved short- and long-term survival compared to fibrinolysis. However, STEMI is still associated with poorer clinical outcomes after PCI, compared to stable CAD, with higher rates of stent thrombosis and an increased risk of myocardial re-infarction persisting throughout long-term follow-up. recent data from randomized controlled trials and meta-analyses demonstrate a consistent and strong signal towards a significant reduction in major adverse cardiac events among patients with STEMI undergoing primary PCI with third-generation DESs, compared with both first-generation and second-generation DESs with durable polymer. Importantly, this signal suggesting superiority of third-generation DESs in patients with STEMI has never been demonstrated with second-generation DESs. Third-generation DESs with enhanced biocompatibility may therefore have a particular clinical benefit in high-risk subgroups of patients with delayed vascular healing but these data warrants confirmation in appropriately designed randomized controlled trials. Objective The purpose of the study is to compare the safety and efficacy of a novel biodegradable-polymer sirolimus-eluting stent (Orsiro®) with a durable-polymer everolimus-eluting stent (Xience Xpedition or Xience Alpine®) in a superiority trial among patients presenting with acute STEMI and undergoing primary PCI. Methods Eligible patients with acute STEMI presenting within 24 hours of symptom onset will undergo primary PCI. At PCI, the randomly allocated stent has to be implanted in the culprit lesion of the target vessel. Patients will be followed-up with a hospital visit at 12 months. Patients will be followed-up for clinical endpoints by telephone at 30 days and 2 years.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease, Acute Coronary Syndrome
Keywords
Percutaneous Coronary Intervention, Stents, Drug-Eluting Stents, Coronary Artery Disease, Acute Coronary Syndrome

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1300 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Orsiro
Arm Type
Active Comparator
Arm Description
Novel biodegradable-polymer sirolimus-eluting stent Orsiro
Arm Title
Xience
Arm Type
Active Comparator
Arm Description
Durable-polymer everolimus-eluting stent Xience
Intervention Type
Device
Intervention Name(s)
Orsiro
Intervention Description
Novel biodegradable-polymer sirolimus-eluting stent used during primary percutaneous coronary intervention
Intervention Type
Device
Intervention Name(s)
Xience
Intervention Description
Durable-polymer everolimus-eluting stent used during primary percutaneous coronary intervention
Primary Outcome Measure Information:
Title
Number of patients with target lesion failure (TLF), a composite of cardiac death, target vessel myocardial infarction (Q-wave and non-Q-wave), or clinically driven target lesion revascularization
Time Frame
up to 12 months
Secondary Outcome Measure Information:
Title
Number of patients with clinically indicated and not clinically indicated target lesion revascularization (TLR)
Time Frame
up to 30 days, 1 and 2 years
Title
Number of patients with clinically indicated and not clinically indicated target vessel revascularization (TVR)
Time Frame
up to 30 days, 1 and 2 years
Title
Number of patients with target vessel failure (TVF)
Time Frame
up to 30 days, 1 and 2 years
Title
Number of patients with cardiac death
Time Frame
up to 30 days, 1 and 2 years
Title
Number of patients with all-cause death (cardiac and non-cardiac)
Time Frame
up to 30 days, 1 and 2 years
Title
Number of patients with myocardial infarction (Q-wave and non-Q-wave)
Time Frame
up to 30 days, 1 and 2 years
Title
Number of patients with definite stent thrombosis
Time Frame
up to 30 days, 1 and 2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥18 years ST-segment elevation acute myocardial infarction Primary PCI occurring within 24 hours of symptom onset Presence of ≥1 acute infarct artery target vessel with one or more coronary artery stenoses in a native coronary artery from 2.25 to 4.0 mm in diameter that can be covered with one or multiple coronary stents Exclusion Criteria Known allergy to aspirin, Ticagrelor, Prasugrel, Clopidogrel, Sirolimus, Everolimus or contrast media Planned surgery within 6 months of primary PCI, unless dual antiplatelet therapy could be maintained throughout the peri-surgical period Currently participating in another trial before reaching the primary endpoint Inability to provide informed consent Non-cardiac comorbid conditions with life expectancy of less than 1 year Mechanical complication of acute myocardial infarction Acute myocardial infarction due to stent thrombosis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thomas Pilgrim, Prof. Dr. med.
Organizational Affiliation
Dep. of Cardiology, Bern University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kantonsspital Aarau
City
Aarau
Country
Switzerland
Facility Name
Universitätsspital Basel
City
Basel
Country
Switzerland
Facility Name
Bern University Hospital, Dep. of Cardiology
City
Bern
ZIP/Postal Code
3010
Country
Switzerland
Facility Name
Universität Freiburg
City
Freiburg
Country
Switzerland
Facility Name
HUG
City
Genf
Country
Switzerland
Facility Name
Lausanne University Hospital
City
Lausanne
ZIP/Postal Code
1011
Country
Switzerland
Facility Name
Kantonsspital Luzern
City
Luzern
Country
Switzerland
Facility Name
Spital Wallis
City
Sion
Country
Switzerland
Facility Name
Kantonsspital St. Gallen
City
St. Gallen
Country
Switzerland
Facility Name
Triemli
City
Zürich
Country
Switzerland

12. IPD Sharing Statement

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A Comparison of an Ultrathin Strut Biodegradable Polymer Sirolimus-Eluting Stent With a Durable Polymer Everolimus-Eluting Stent for Patients With Acute ST-Segment Elevation Myocardial Infarction Undergoing Primary Percutaneous Coronary Intervention

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