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Anatomical sNuffbox for Coronary anGiography and IntervEntions

Anatomical sNuffbox for Coronary anGiography and IntervEntions

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03986151
Acronym
ANGIE
Enrollment
1042
Registered
2019-06-14
Start date
2019-06-11
Completion date
2021-02-20
Last updated
2021-03-12

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

Conditions

Coronary Artery Disease, Vascular Access Complication

Keywords

coronary angiography, radial access, distal radial access, anatomical snuffbox, radial artery occlusion

Brief summary

This randomized, single-center, prospective study seeks to compare the conventional radial approach with the recently described distal radial approach (anatomical snuffbox) concerning the patency of the radial artery in patients subjected to coronary angiography or percutaneous coronary intervention.

Detailed description

Transradial approach has become the standard approach for coronary angiography (CAG) and percutaneous coronary intervention (PCI). The current ESC/EACTS guidelines of myocardial revascularization support using radial approach (RA) rather than femoral approach (FA) if the operators are experts for RA. Recently, an alternative transradial access has been suggested at the anatomical snuffbox, with potential additional benefits including a reduction in radial artery occlusion rate (which allows reintervention through the same access site and potential use as a graft), a decrease in other local vascular complications, shorter hemostasis duration, patients' intra and post procedural comfort and shorter recovery time. However, the feasibility of PCI via snuffbox approach is still concerned due to the lack of data. Therefore, the aim of the study is to compare the two approaches concerning the patency of the radial artery ≥30 days after the intervention with Doppler in a randomized way. Due to the anastomosis of the distal radial artery with the superficial palmar arch, even in case of total radial artery occlusion within the anatomical snuffbox, the antegrade blood flow may be preserved and, therefore, decreased incidents of radial artery occlusion are expected in the right distal radial artery approach group. The mean diameter of radial artery at the anatomical snuffbox is 2.4 mm, whereas the mean diameter of the radial artery at the forearm is 2.7 mm, and this could potentially contribute to shorter hemostasis duration.

Interventions

Comparison of the conventional radial approach with the distal radial approach (anatomical snuffbox)

Sponsors

University Hospital of Patras
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Indication for coronary angiography * Informed consent

Exclusion criteria

* Non palpable right radial artery * Prior complicated right transradial intervention (radial artery dissection, perforation, occlusion) * Prior CABG * STEMI * Hemodynamic instability * Anatomical restrictions (fistula, etc)

Design outcomes

Primary

MeasureTime frame
Rate of right radial artery occlusion≥30 days after CAG or PCI

Secondary

MeasureTime frameDescription
Duration of sheath insertion procedureImmediately post-procedurally
Rate of successful completion of coronary angiographyImmediately post-procedurally
Rate of successful completion of percutaneous coronary interventionImmediately post-procedurally
Total Contrast volumeImmediately post-procedurally
Total Fluoroscopy timeImmediately post-procedurally
Rate of successful insertion of the sheathImmediately post-procedurally
Total Procedure TimeImmediately post-procedurally
Time required for hemostasis1-6 hours
Postprocedural Hematoma (modified EASY class)3 hours
Rate of distal radial artery occlusion≥30 days after CAG or PCI
Pain associated with the procedure: Pain scale 0-101 hourPain scale 0-10. A visual anlog pain scale 0-10 will be shown to the patient post-precedurally. 0=no pain, 10=worst pain. Patient will be asked to report the severity of the pain associated with the procedure.
Total Radiation DoseImmediately post-procedurally

Countries

Greece

Outcome results

None listed

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