Use of Glidesheath Slender to Reduce Radial Artery Occlusion Following 7 French Transradial Coronary Intervention
Primary Purpose
Radial Artery Occlusion, Coronary Artery Disease
Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
7-Fr Glidesheath Slender
Cordis 7-Fr radial sheath
Sponsored by
About this trial
This is an interventional prevention trial for Radial Artery Occlusion focused on measuring Radial artery occlusion, 7-Fr radial sheath, Transradial Coronary Intervention
Eligibility Criteria
Inclusion Criteria:
- Patients undergoing coronary PCI via 7-Fr transradial approach
- Informed consent
- the patency of radial artery confirmed by ultrasound
Exclusion Criteria:
- The abnormal of radial artery confirmed by ultrasound
- Previous failed radial access.
- Known bleeding disorder or hypercoagulable condition
- Cardiogenic shock
Sites / Locations
- Fuwai Hospital National Center for Cardiovascular Diseases
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Glidesheath Slender
Standard sheath
Arm Description
The transradial procedure will be performed using the 7-Fr glidesheath slender (studied sheath)
The transradial procedure will be performed using the standard 7- French radial sheath (comparator sheath)
Outcomes
Primary Outcome Measures
Radial artery occlusion
Evaluated clinically and by ultrasound
Secondary Outcome Measures
Vascular access site complications
Includes: bleeding or hematoma, pseudoaneurysm, artery dissection, arteriovenous fistula, compartment syndrome of the forearm
Radial artery spasm
Radial artery spasm
Procedure success
completion of the planned procedure through the initially selected radial access route
The degree of pain at the puncture site
Scored on a scale of 1-10 scoring system
Full Information
NCT ID
NCT04748068
First Posted
January 25, 2021
Last Updated
February 8, 2021
Sponsor
China National Center for Cardiovascular Diseases
1. Study Identification
Unique Protocol Identification Number
NCT04748068
Brief Title
Use of Glidesheath Slender to Reduce Radial Artery Occlusion Following 7 French Transradial Coronary Intervention
Official Title
Use of Glidesheath Slender to Reduce Radial Artery Occlusion Following 7 French Transradial Coronary Intervention
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Unknown status
Study Start Date
February 1, 2021 (Anticipated)
Primary Completion Date
May 31, 2021 (Anticipated)
Study Completion Date
May 31, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
China National Center for Cardiovascular Diseases
4. Oversight
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
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The objective of this study is to determine the rate of early radial artery occlusion following 7-French(7-Fr) transradial coronary intervention using a new Terumo (Tokyo, Japan) Glidesheath Slender, in comparison with the currently used 7-Fr radial sheath.
Detailed Description
Based on previously reported studies the rates of radial artery occlusion using a standard 7-Fr sheath is around 12%, compared to the previous studies of the Glidesheath Slender (see reference in the citations), the rate of radial artery occlusion was reported less than 5%. To prove Slender sheaths are superior to traditional ones, the sample size was estimated according to this, the class I error (α) is set as 0.05 on both sides, and the test efficiency (β) is set as 80%, then at least 248 patients are needed in each group.
This study will be a prospective randomized, single-blinded (patient-blinded) study, comparing the rate of radial artery occlusion between the 7-Fr Glidesheath Slender (Terumo, Japan) and the standard 7-Fr radial sheath (cordis, USA) in patients undergoing complex transradial coronary intervention.
The study will enroll patients who will undergo elective complex percutaneous coronary intervention (PCI) via 7-Fr transradial approach at Fuwai Hospital National Center for Cardiovascular Diseases.
A baseline clinical vascular & ultrasound assessment will be performed prior to the procedure to document patency of the radial artery.
Patients will be randomized in 1:1 fashion to either receive the 7-Fr Terumo Glidesheath Slender versus the currently used 7-Fr sheath.
The standard angiogram/ PCI will be performed as per usual practice. Following the PCI, clinical vascular assessment as well as an ultrasound will be performed prior to discharge.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Radial Artery Occlusion, Coronary Artery Disease
Keywords
Radial artery occlusion, 7-Fr radial sheath, Transradial Coronary Intervention
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
500 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Glidesheath Slender
Arm Type
Experimental
Arm Description
The transradial procedure will be performed using the 7-Fr glidesheath slender (studied sheath)
Arm Title
Standard sheath
Arm Type
Active Comparator
Arm Description
The transradial procedure will be performed using the standard 7- French radial sheath (comparator sheath)
Intervention Type
Device
Intervention Name(s)
7-Fr Glidesheath Slender
Other Intervention Name(s)
Glidesheath Slender, Terumo, Tokyo, Japan
Intervention Description
The 7 Fr Glidesheath Slender is a recently developed thin-walled radial sheath. It combines an ID of 2.46 mm, with an OD of 2.79 mm, representing thereby the thinnest 7 Fr sheath currently available on the market
Intervention Type
Device
Intervention Name(s)
Cordis 7-Fr radial sheath
Intervention Description
Avanti+ Catheter Sheath Introducer, Cordis, USA, outer diameter: 3.02 mm
Primary Outcome Measure Information:
Title
Radial artery occlusion
Description
Evaluated clinically and by ultrasound
Time Frame
24 hours
Secondary Outcome Measure Information:
Title
Vascular access site complications
Description
Includes: bleeding or hematoma, pseudoaneurysm, artery dissection, arteriovenous fistula, compartment syndrome of the forearm
Time Frame
24 hours
Title
Radial artery spasm
Description
Radial artery spasm
Time Frame
24 hours
Title
Procedure success
Description
completion of the planned procedure through the initially selected radial access route
Time Frame
24 hours
Title
The degree of pain at the puncture site
Description
Scored on a scale of 1-10 scoring system
Time Frame
24 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients undergoing coronary PCI via 7-Fr transradial approach
Informed consent
the patency of radial artery confirmed by ultrasound
Exclusion Criteria:
The abnormal of radial artery confirmed by ultrasound
Previous failed radial access.
Known bleeding disorder or hypercoagulable condition
Cardiogenic shock
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hao Wang, MD,PhD
Phone
+86-15701277767
Email
wanghao_fuwai@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kefei Dou, MD,PhD
Organizational Affiliation
Fuwai Hospital National Center for Cardiovascular Diseases
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Chenggang Zhu, MD,PhD
Organizational Affiliation
Fuwai Hospital National Center for Cardiovascular Diseases
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fuwai Hospital National Center for Cardiovascular Diseases
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100037
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hao Wang, MD,PhD
Phone
+86-15701277767
Email
wanghao_fuwai@126.com
First Name & Middle Initial & Last Name & Degree
Kefei Dou, MD,PhD
First Name & Middle Initial & Last Name & Degree
Chenggang Zhu, MD,PhD
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
26811162
Citation
Rashid M, Kwok CS, Pancholy S, Chugh S, Kedev SA, Bernat I, Ratib K, Large A, Fraser D, Nolan J, Mamas MA. Radial Artery Occlusion After Transradial Interventions: A Systematic Review and Meta-Analysis. J Am Heart Assoc. 2016 Jan 25;5(1):e002686. doi: 10.1161/JAHA.115.002686.
Results Reference
background
PubMed Identifier
31753298
Citation
Bernat I, Aminian A, Pancholy S, Mamas M, Gaudino M, Nolan J, Gilchrist IC, Saito S, Hahalis GN, Ziakas A, Louvard Y, Montalescot G, Sgueglia GA, van Leeuwen MAH, Babunashvili AM, Valgimigli M, Rao SV, Bertrand OF; RAO International Group. Best Practices for the Prevention of Radial Artery Occlusion After Transradial Diagnostic Angiography and Intervention: An International Consensus Paper. JACC Cardiovasc Interv. 2019 Nov 25;12(22):2235-2246. doi: 10.1016/j.jcin.2019.07.043.
Results Reference
background
PubMed Identifier
27567021
Citation
Aminian A, Iglesias JF, Van Mieghem C, Zuffi A, Ferrara A, Manih R, Dolatabadi D, Lalmand J, Saito S. First prospective multicenter experience with the 7 French Glidesheath slender for complex transradial coronary interventions. Catheter Cardiovasc Interv. 2017 May;89(6):1014-1020. doi: 10.1002/ccd.26773. Epub 2016 Aug 27.
Results Reference
background
PubMed Identifier
32863791
Citation
Isawa T, Horie K, Honda T, Taguri M, Tada N. Slender Sheath/Guiding Catheter Combination vs. Sheathless Guiding Catheter for Acute Coronary Syndrome: A Propensity-Matched Analysis of the Two Devices. J Interv Cardiol. 2020 Aug 14;2020:8216831. doi: 10.1155/2020/8216831. eCollection 2020. Erratum In: J Interv Cardiol. 2020 Oct 22;2020:1303764.
Results Reference
background
PubMed Identifier
10348538
Citation
Saito S, Ikei H, Hosokawa G, Tanaka S. Influence of the ratio between radial artery inner diameter and sheath outer diameter on radial artery flow after transradial coronary intervention. Catheter Cardiovasc Interv. 1999 Feb;46(2):173-8. doi: 10.1002/(SICI)1522-726X(199902)46:23.0.CO;2-4.
Results Reference
background
PubMed Identifier
26839392
Citation
Costa F, van Leeuwen MA, Daemen J, Diletti R, Kauer F, van Geuns RJ, Ligthart J, Witberg K, Zijlstra F, Valgimigli M, Van Mieghem NM. The Rotterdam Radial Access Research: Ultrasound-Based Radial Artery Evaluation for Diagnostic and Therapeutic Coronary Procedures. Circ Cardiovasc Interv. 2016 Feb;9(2):e003129. doi: 10.1161/CIRCINTERVENTIONS.115.003129.
Results Reference
background
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Use of Glidesheath Slender to Reduce Radial Artery Occlusion Following 7 French Transradial Coronary Intervention
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