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Arterial Access for Coronary Intervention in Myocardial Infarction

Femoral Versus Radial Access for Coronary Intervention in the Acute Phase of ST-Elevation Myocardial Infarction

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00356044
Enrollment
439
Registered
2006-07-25
Start date
2004-05-31
Completion date
2005-12-31
Last updated
2007-07-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Angioplasty, Transluminal, Percutaneous Coronary, Myocardial Infarction, Myocardial Reperfusion

Keywords

Transradial access, Femoral access, Femoral vs radial access

Brief summary

The aim of this study is to compare the radial and femoral access for percutaneous interventions in the acute phase of the ST elevation acute myocardial infarction in terms of efficacy and security.

Detailed description

Some groups have previously used the radial artery as the access route in the procedures of percutaneous coronary revascularization, with good results. The advantages of the radial compared with femoral access are related to a lower incidence of vascular complications. The radial access has also inconveniences such as a less predictable anatomy which can make the procedure difficult and prolong the time required.The patients with ST elevation myocardial infarction have an increased risk of vascular complications after interventional procedures because previous antithrombotic or thrombolytic therapy.On the other hand, the time and success of the procedure are significant prognostic issues.In this sitting, the radial approach might reduce vascular complications and increase other cardiovascular events when comparing with the classical femoral access. For this reason, the purpose of the study is to compare both arterial access in terms of efficacy and security and to quantify the consequences of the advantages and drawbacks of both.

Interventions

PROCEDURECoronary angioplasty

Sponsors

Hospital Juan Canalejo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients with ST elevation acute myocardial infarction referred for primary,facilitated or of rescue coronary angioplasty in the first 12 hours since the start of the symptoms.

Exclusion criteria

* Patients in cardiogenic shock were excluded following operator criteria. * Previous coronary surgery with mammary artery graft * Coronary artery intervention in the previous month * Absolute or relative contraindication for access via the radial artery route:Radial pulse absent or weak, abnormal Allen test,anatomy known to impede the use of the radial route or hemodialysis or advanced chronic renal insufficiency (creatinine \>3 mg/dl). * Patients with absolute or relative contraindication for the use of the femoral route. * Absence of informed consent from the patient

Design outcomes

Primary

MeasureTime frame
All cause mortality at 30 dayswithin the first 30 days (plus or minus 5 days) after the index myocardial infarction
New ST elevation acute myocardial infarction at 30 dayswithin the first 30 days (plus or minus 5 days) after the index myocardial infarction
Coronary revascularization as a result of recurrent ischemia at 30 dayswithin the first 30 days (plus or minus 5 days) after the index myocardial infarction
Major vascular complications at 30 days.within the first 30 days (plus or minus 5 days) after the index myocardial infarction

Secondary

MeasureTime frame
Hospital stay
Embolic stroke at 30 dayswithin the first 30 days (plus or minus 5 days) after the index myocardial infarction
Estimation of costs
Coronary revascularization at 30 dayswithin the first 30 days (plus or minus 5 days) after the index myocardial infarction
Cardiovascular mortality at 30 dayswithin the first 30 days (plus or minus 5 days) after the index myocardial infarction
Procedural time

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026