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Femoral Versus Radial Access for Primary PCI (SAFARI-STEMI)

Primary Purpose

Myocardial Infarction, STEMI

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Primary Percutaneous Coronary Intervention (PPCI)
Sponsored by
Ottawa Heart Institute Research Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Myocardial Infarction focused on measuring ST-Elevation Myocardial Infarction, Mortality

Eligibility Criteria

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

Inclusion Criteria:

  1. Ischemic chest discomfort of greater or equal to 30 minutes duration,
  2. Onset of chest pain of greater or equal to 12 hrs prior to entry into the study,
  3. ST segment elevation of > 1 mm (0.1 mV) in two or more contiguous electrocardiographic leads (on a standard 12 lead ECG) or left bundle branch block not known to be old

Exclusion Criteria:

  1. Age < 18 yrs
  2. Active bleeding
  3. Inadequate vascular access from the femoral arteries (i.e. severe peripheral vascular artery disease precluding right or left femoral approach)
  4. Abnormal Allen's test precluding either right or left radial approach
  5. PCI within the last 30 days
  6. Fibrinolytic agents within the last 7 days
  7. Warfarin, dabigatran or other oral anticoagulant within the last 7 days
  8. Known coagulation disorder (i.e. INR >2.0, platelets <100,000 / mm3)
  9. Allergy to aspirin
  10. Participation in a study with another investigational device or drug < four weeks
  11. Known severe renal impairment (creatinine >200 umol/L)*
  12. Known severe contrast (dye) allergy
  13. Prior coronary artery bypass surgery
  14. Inability to provide informed consent

    • Bivalirudin is contraindicated in renal failure.

Sites / Locations

  • St. Boniface Hospital
  • Saint John Regional Hospital
  • Queen Elizabeth II Health Sciences Center
  • University of Ottawa Heart Institute
  • Thunder Bay Regional Health Sciences Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

TRA

TFA

Arm Description

Transradial Access

Transfemoral Access

Outcomes

Primary Outcome Measures

All-cause mortality
The primary outcomes will be all-cause mortality measured at 30 days.

Secondary Outcome Measures

Death, reinfarction, or stroke
All-cause mortality
Reinfarction
Stroke
Stent thrombosis
Bleeding
Number of blood transfusions
Cardiogenic shock
Critical time intervals (including door-to-balloon time)
Fluoroscopy time and radiation exposure
Length of Hospital Stay
Resource utilization

Full Information

First Posted
July 13, 2011
Last Updated
January 25, 2019
Sponsor
Ottawa Heart Institute Research Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT01398254
Brief Title
Femoral Versus Radial Access for Primary PCI
Acronym
SAFARI-STEMI
Official Title
The Safety and Efficacy of Femoral Access Versus Radial for Primary Percutaneous Coronary Intervention in ST-Elevation Myocardial Infarction (SAFARI-STEMI Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
July 2011 (undefined)
Primary Completion Date
December 2018 (Actual)
Study Completion Date
January 16, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ottawa Heart Institute Research Corporation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Primary percutaneous coronary intervention (PPCI) has become the dominant strategy for the treatment of ST-elevation myocardial infarction (STEMI), as studies have shown that PPCI is superior to fibrinolytic therapy. Recent evidence suggests that transradial access (TRA) is superior to transfemoral (TFA) for patients undergoing PPCI. Two large trials report a mortality benefit favouring TRA. The results of these two trials could significantly impact practice guidelines and lead to a recommendation that the approach of choice for primary PCI be radial rather than femoral. This would have significant implications for both PCI centers and interventionalists associated with a large impact on practice and education. Yet, many centers and interventionalists in Canada and in the USA prefer TFA and currently feel pressured in making the change to TRA. With that said, these trials did not include new pharmacotherapy and new technology that would likely have closed or eliminated the gap between TFA and TRA by improving the safety and efficacy of these two approaches. Furthermore, these trials were not powered to conclusively show a mortality benefit. The authors of the two large trials emphasized the need for further trials to confirm the benefits of TRA. The SAFARI-STEMI trial aims to compare TFA with TRA in patients undergoing primary percutaneous intervention (PPCI). The primary outcome will be defined as all cause mortality measured at 30 days. The trial will also evaluate: 1) bleeding events and 2) the composite of death, reinfarction, or stroke defined as major adverse clinical events (MACE). The trial will include the use of antithrombotic therapy with monotherapy, with either bivalirudin or unfractionated heparin; the use of glycoprotein inhibitors IIb/IIIa inhibitors will be avoided. The study will encourage liberal use of vascular closing devices. The trial will also compare delays to reperfusion between the two strategies. Finally, a cost analysis is proposed. In view of recent publications, there is now a need for a large randomized trial using contemporary adjunct therapies to assess the safety and efficacy of the TRA vs. the TFA in PPCI. The proposed trial aims to conclusively show whether there is a survival benefit associated with the TRA approach.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myocardial Infarction, STEMI
Keywords
ST-Elevation Myocardial Infarction, Mortality

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2292 (Actual)

8. Arms, Groups, and Interventions

Arm Title
TRA
Arm Type
Other
Arm Description
Transradial Access
Arm Title
TFA
Arm Type
Other
Arm Description
Transfemoral Access
Intervention Type
Procedure
Intervention Name(s)
Primary Percutaneous Coronary Intervention (PPCI)
Intervention Description
Participants will be randomly assigned an access site, radial or femoral, for PPCI.
Primary Outcome Measure Information:
Title
All-cause mortality
Description
The primary outcomes will be all-cause mortality measured at 30 days.
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Death, reinfarction, or stroke
Time Frame
30 days and 6 months
Title
All-cause mortality
Time Frame
6 months
Title
Reinfarction
Time Frame
30 days and 6 months
Title
Stroke
Time Frame
30 days and 6 months
Title
Stent thrombosis
Time Frame
30 days and 6 months
Title
Bleeding
Time Frame
30 days
Title
Number of blood transfusions
Time Frame
30 days
Title
Cardiogenic shock
Time Frame
30 days
Title
Critical time intervals (including door-to-balloon time)
Time Frame
Index hospitalization
Title
Fluoroscopy time and radiation exposure
Time Frame
Index Catheterization
Title
Length of Hospital Stay
Time Frame
Index hospitalization
Title
Resource utilization
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Ischemic chest discomfort of greater or equal to 30 minutes duration, Onset of chest pain of greater or equal to 12 hrs prior to entry into the study, ST segment elevation of > 1 mm (0.1 mV) in two or more contiguous electrocardiographic leads (on a standard 12 lead ECG) or left bundle branch block not known to be old Exclusion Criteria: Age < 18 yrs Active bleeding Inadequate vascular access from the femoral arteries (i.e. severe peripheral vascular artery disease precluding right or left femoral approach) Abnormal Allen's test precluding either right or left radial approach PCI within the last 30 days Fibrinolytic agents within the last 7 days Warfarin, dabigatran or other oral anticoagulant within the last 7 days Known coagulation disorder (i.e. INR >2.0, platelets <100,000 / mm3) Allergy to aspirin Participation in a study with another investigational device or drug < four weeks Known severe renal impairment (creatinine >200 umol/L)* Known severe contrast (dye) allergy Prior coronary artery bypass surgery Inability to provide informed consent Bivalirudin is contraindicated in renal failure.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michel R Le May, MD
Organizational Affiliation
Ottawa Heart Institute Research Corporation
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Boniface Hospital
City
Winnipeg
State/Province
Manitoba
ZIP/Postal Code
R2H 2A6
Country
Canada
Facility Name
Saint John Regional Hospital
City
Saint John
State/Province
New Brunswick
ZIP/Postal Code
E2L 4L2
Country
Canada
Facility Name
Queen Elizabeth II Health Sciences Center
City
Halifax
State/Province
Nova Scotia
ZIP/Postal Code
B3H 4G4
Country
Canada
Facility Name
University of Ottawa Heart Institute
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1Y 4W7
Country
Canada
Facility Name
Thunder Bay Regional Health Sciences Center
City
Thunder Bay
State/Province
Ontario
ZIP/Postal Code
P7B 6V4
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
33422518
Citation
Marbach JA, Wells G, Santo PD, So D, Chong AY, Russo J, Labinaz M, Dick A, Froeschl M, Glover C, Hibbert B, Marquis JF, MacDougall A, Kass M, Paddock V, Quraishi AUR, Chandrasekhar J, Ghosh N, Bernick J, Le May M. Acute kidney injury after radial or femoral artery access in ST-segment elevation myocardial infarction: AKI-SAFARI. Am Heart J. 2021 Apr;234:12-22. doi: 10.1016/j.ahj.2020.12.019. Epub 2021 Jan 7.
Results Reference
derived
PubMed Identifier
31895439
Citation
Le May M, Wells G, So D, Chong AY, Dick A, Froeschl M, Glover C, Hibbert B, Marquis JF, Blondeau M, Osborne C, MacDougall A, Kass M, Paddock V, Quraishi A, Labinaz M. Safety and Efficacy of Femoral Access vs Radial Access in ST-Segment Elevation Myocardial Infarction: The SAFARI-STEMI Randomized Clinical Trial. JAMA Cardiol. 2020 Feb 1;5(2):126-134. doi: 10.1001/jamacardio.2019.4852. Erratum In: JAMA Cardiol. 2020 Feb 1;5(2):236. JAMA Cardiol. 2020 Sep 1;5(9):1071.
Results Reference
derived

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Femoral Versus Radial Access for Primary PCI

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