Safety and Feasibility of the Infinity Catheter for Radial Access

Rutgers The State University of New Jersey logo

Rutgers The State University of New Jersey

Status

Completed

Conditions

Carotid Stenosis
Brain Tumor
Brain Aneurysm
Stroke, Acute
Cavernous Sinus Thrombosis
Intracranial Arteriovenous Malformations

Treatments

Device: Transradial approach

Study type

Observational

Funder types

Other

Identifiers

NCT04553549
Pro2020000869

Details and patient eligibility

About

The main objective of this single arm study is to evaluate the safety and feasibility of the AXS Infinity LS (Stryker, Freemont, CA, USA) and AXS Infinity LS Plus (Stryker, Freemont, CA, USA) catheters during the transradial approach through a secondary use of the data collected during neurointerventional procedures. This includes evaluating the conversion rates to a transfemoral approach. A secondary aim of the study is to assess the radial artery occlusion rates post procedure.

Full description

Patients who are undergoing endovascular intervention will be enrolled into the study. Consent will be obtained for the procedure and for the use of their prospectively collected clinical data. As the metrics analyzed in this study are already normally collected, this study can be considered as a secondary use of the data. The procedure will be done using standard criteria as per operator preference. All interventional cases at the study institution undergo a "radial first" approach, meaning that the access site of choice is the radial artery. The investigators will measure the radial artery size to ensure that the artery is greater than 2.4 mm in order to use the Infinity catheter (8Fr). If the artery does not meet the size criteria, only a 6Fr sheath will be used, and the data recorded during the procedure will not be utilized for analysis in this study. The preoperative and postoperative care will be the same for all the patients. No tests will be done outside of standard of care.

Enrollment

80 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age group 18 years and above.
  • Patients undergoing neuro-embolization using large bore catheters

Exclusion criteria

  • Patients with Radial artery diameter less than 2.4 mm measured with Ultrasound
  • Age<18
  • Patients who have previous surgeries at either approach site which precludes the use of one of the approach sites
  • Patients who has poor collateral circulation, Raynaud's phenomenon, radial loop, brachial or subclavian stenosis, aberrant origin of the subclavian artery
  • Pregnant patients

Trial design

80 participants in 1 patient group

Transradial approach
Description:
The procedure will be done using standard criteria as per operator preference. All interventional cases at our institution undergo a "radial first" approach, meaning that the access site of choice is the radial artery. The investigators will measure the radial artery size to ensure that the artery is greater than 2.4 mm in order to use the Infinity catheter (8Fr).
Treatment:
Device: Transradial approach

Trial documents
2

Trial contacts and locations

0

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Central trial contact

Priyank Khandelwal, MD

Data sourced from clinicaltrials.gov

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