RADVES: Radifocus (Terumo) Versus Silverway (Asahi) to Deliver Catheters During Cardiac Catheterization

Sponsor
Ziekenhuis Oost-Limburg (Other)
Overall Status
Completed
CT.gov ID
NCT05231889
Collaborator
(none)
100
1
2
4.8
20.7

Study Details

Study Description

Brief Summary

In some cases the standard J-tip guidewire cannot deliver the catheter into the aortic root, because of arterial loops or spasm. In these cases a hydrophilic guidewire (Terumo) gives the right lubricity and good shape retention to guide the catheter through the artery. However, the Terumo wire does not give much torque and could therefore easily penetrate side branches and cause dissection or perforation. The latest Silverway guidewire has some new advantages which is easier to guide and could cause less complications while faster delivery of catheters to the aortic valve. The investigators aim to compare both guide wires.

Condition or Disease Intervention/Treatment Phase
  • Device: Silverway guidewire
  • Device: Radifocus guidewire
N/A

Detailed Description

During cardiac catheterization a catheter is threaded through the radial arteries to the aortic root with the support of a guide wire. The standard workhorse to deliver the catheter is a J-tip guidewire (spring coil wire). However, in patients with arterial tortuosity or spasm, this guidewire has low lubricity and no torque to direct the catheter because the outer coil and core are not connected together.

If this problem is encountered, interventional cardiologists will use a hydrophilic polymer-coated guide wire. Up to date there are several hydrophilic coated guide wires available. One of these is the Radifocus Guide Wire M (Terumo, Japan). Although it has better torque transmission than the spring wire, it still has low torque transmission due to a Nitinol core structure, is less supportive and can easily enter side branches because of the high lubricity and therefore might cause dissections or perforations.

In some cases, coronary angioplasty guide wires are needed to negotiate a highly tortuous artery, but they lack the support to advance the catheter.

Recently, the Silverway Guide Wire has been created (Asahi Intecc Co, LTD., Japan) to overcome the problems that a spring- and polymer wire have. Features that this new guide wire provide is hybrid coating and ACT ONE technology that connects the wire core and coil to ensure one to one torque transmission The investigators aim to compare both guide wires in deliverability, workability and complication rate.

Study Design

Study Type:
Interventional
Actual Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Supportive Care
Official Title:
Radifocus (Terumo) Versus Silverway (Asahi) to Deliver Catheters During Cardiac Catheterization
Actual Study Start Date :
Feb 15, 2022
Actual Primary Completion Date :
Jul 12, 2022
Actual Study Completion Date :
Jul 12, 2022

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Below the shoulder vascular anomaly

If the standard J-tip guidewire does not cross a vascular anomaly located below the shoulder

Device: Radifocus guidewire
The Radifocus guidewire is a hydrophilic coated guidewire that is used when a standard J-tip guidewire does not cross a vascular anomaly

Active Comparator: Above the shoulder vascular anomaly

If the standard J-tip guidewire does not cross a vascular anomaly located above the shoulder

Device: Silverway guidewire
The Silverway guidewire is a newly developed guidewire to overcome the problems the Radifocus guidewire has

Outcome Measures

Primary Outcome Measures

  1. Time in seconds from introduction to aortic root [During procedure]

    Measuring time from entering the guidewire in the catheter to delivery of the catheter to the aortic root (in seconds)

Secondary Outcome Measures

  1. The ability of the study wire to deliver the catheter to the aortic root [During procedure]

    If the study wire is able to deliver the catheter to the aortic root

  2. Change of access site [During procedure]

    Is change of access site necessary?

  3. Interventional cardiologists' survey of grading parameters working with the guide wire [Directly after procedure. Scale: not satisfactory (1) - somewhat satisfactory (2) - satisfactory (3)]

    The interventional cardiologist who used the study wire must fill up a survey after procedure to grade the workability and deliverability of the study wire

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Indication for radial artery access for diagnostic cardiac catheterization

  • Being able to receive the per standard protocol Verapamil and Nitroglycerin administration via radial artery

  • Not able to deliver a diagnostic or guiding catheter to the aortic root by means of the standard J tip wire

  • No signs of early complication after initial attempt with the J tip wire such as dissection, perforation or hematoma

  • Age ≥ 18 years

Exclusion Criteria:
  • Femoral or brachial artery access

  • Patients with known CREST syndrome or other forms of scleroderma

  • Emergent indication for cardiac catheterization such as an acute coronary syndrome

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ziekenhuis Oost-Limburg Genk Limburg Belgium 3600

Sponsors and Collaborators

  • Ziekenhuis Oost-Limburg

Investigators

  • Principal Investigator: Koen Ameloot, Dr., Ziekenhuis Oost-Limburg

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Koen Ameloot, Medical doctor, Principal Investigator, Ziekenhuis Oost-Limburg
ClinicalTrials.gov Identifier:
NCT05231889
Other Study ID Numbers:
  • Z-2021119
First Posted:
Feb 9, 2022
Last Update Posted:
Jul 14, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Koen Ameloot, Medical doctor, Principal Investigator, Ziekenhuis Oost-Limburg
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 14, 2022