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Completed

NCT Number: NCT01398254

Femoral Versus Radial Access for Primary PCI

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

St. Boniface Hospital, Winnipeg, Manitoba, Canada

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Primary Percutaneous Coronary Intervention (PPCI)

Procedure

Participants will be randomly assigned an access site, radial or femoral, for PPCI.

Primary outcomes

  1. All-cause mortality

    Time frame: 30 days

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

Secondary outcomes

  1. Death, reinfarction, or stroke

    Time frame: 30 days and 6 months

  2. All-cause mortality

    Time frame: 6 months

  3. Reinfarction

    Time frame: 30 days and 6 months

  4. Stroke

    Time frame: 30 days and 6 months

  5. Stent thrombosis

    Time frame: 30 days and 6 months

  6. Bleeding

    Time frame: 30 days

  7. Number of blood transfusions

    Time frame: 30 days

  8. Cardiogenic shock

    Time frame: 30 days

  9. Critical time intervals (including door-to-balloon time)

    Time frame: Index hospitalization

  10. Fluoroscopy time and radiation exposure

    Time frame: Index Catheterization

  11. Length of Hospital Stay

    Time frame: Index hospitalization

  12. Resource utilization

    Time frame: 30 days

Sponsors and collaborators

Lead sponsor

Ottawa Heart Institute Research Corporation

Other

Registry information

Official study title

The Safety and Efficacy of Femoral Access Versus Radial for Primary Percutaneous Coronary Intervention in ST-Elevation Myocardial Infarction (SAFARI-STEMI Trial)

Acronym: SAFARI-STEMI

Important dates

Study start
2011
Primary completion
2018
Study completion
2019
First posted
Jul 20, 2011
Registry last updated
Jan 29, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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