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Radial Artery Occlusion and Dual Artery Hemostasis After Transradial Approach.

Radial Artery Occlusion

* Improving patient comfort and implementing the protocols required to minimize the risk of RAO must be part of quality control.
* Several procedural parameters are related to the risk of RAO but hemostasis is a critical period.
* Despite the fact that non-occlusive hemostasis of the radial artery is a recognized and effective technique for reducing the risk of RAO, it is rarely practiced because it is tedious, involves additional care and is not always effective with current hemostasis systems.
* Prophylactic compression of the cubital artery during radial artery hemostasis has been shown to be effective in maintaining non-occlusive hemostasis but requires 2 devices and does not simplify care procedures.
* The Terry2™ band is a new dual device that offers effortless non-occlusive radial hemostasis and does not require repeated intervention by nursing staff.

The primary objectives of this observational study are to demonstrate the benefits, safety and impact on care of using Terry2™ band in patients undergoing diagnostic or interventional catheterization by radial (or ulnar) approach.

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Conditions de participation

  • Sexe:

    ALL

  • Âges admissibles:

    18 and up

Critères de participation

Inclusion Criteria:

* Any patient referred for diagnostic or interventional catheterization through radial or cubital approach

Exclusion Criteria:

* Unable to understand the study design and sign an informed consent
* Unable to receive antiplatelet therapy with aspirin and/or clopidogrel-prasugrel and/or ticagrelor and intravenous anticoagulant treatment with heparin or bivalirudin
* Presence of any local conditions like hematoma or pseudo-aneurysms precluding radial or cubital access.
* Presence of PPG while simultaneously compressing the radial and cubital arteries (due to collateral branches or interosseous artery), which prevents the establishment of non-occlusive hemostasis with the Terry2(TM) band.

Lieu de l'étude

IUCPQ - Laval Hospital
IUCPQ - Laval Hospital
Québec, Quebec
Canada

Contactez l'équipe d'étude

Primary Contact

Tomas A Cieza Lara, MD

CHU de Québec
CHU de Québec
Québec, Quebec
Canada

Contactez l'équipe d'étude

Primary Contact

Jimmy MacHaalany

CSSS Chicoutimi
CSSS Chicoutimi
Chicoutimi, Quebec
Canada

Contactez l'équipe d'étude

Primary Contact

Francis Bonenfant

Hôpital Sainte-Marie
Hôpital Sainte-Marie
Trois-Rivières, Quebec
Canada

Contactez l'équipe d'étude

Primary Contact

Vincent Spagnoli, MD

CHUM- Centre hospitalier de l'Université de Montréal
CHUM- Centre hospitalier de l'Université de Montréal
Montréal, Quebec
Canada

Contactez l'équipe d'étude

Primary Contact

Samer Mansour

Backup Contact

Adriana Carbonaro

Étude parrainée par
Laval University
Participants recherchés
Plus d'informations
ID de l'étude: NCT04933136