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Relation Among Shear Stress Distribution, Stent Design, and Subsequent Vessel Healing After Drug-eluting Stent Implantation (SHEAR DES)

Primary Purpose

Coronary Heart Disease

Status
Unknown status
Phase
Phase 4
Locations
Japan
Study Type
Interventional
Intervention
Promus element, Xience prime, and Nobori
Sponsored by
Kobe University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Heart Disease focused on measuring Shear stress, Optical coherence tomography, Drug-eluting stents

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Older than 20 years old.
  • Indication of PCI with Xience prime, Nobori, or Promus element.
  • Clinical diagnosis of stable angina, unstable angina or silent ischemia with reference vessel diameters ranging from 2.5-3.5mm.
  • Underwent CT angiography before PCI.
  • To agree to review and record all the clinical course in this research protocol.

Exclusion Criteria:

  • Previous history of pancytopenia, liver function, renal dysfunction, hypersensitive history of the drug.
  • Low ejection fraction (LVEF<=30%), an impaired liver function, and renal dysfunction (eGFR<=40)
  • Severe calcification
  • Stent restenosis

Sites / Locations

  • Kobe University Graduate School of MedicineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Active Comparator

Arm Label

Promus element

Xience Prime

Nobori

Arm Description

Promus element is a thin struts, 2-link design, evelolimus-eluting stents.

Xience Prime is a thin struts, 3-link design, evelolimus-eluting stents.

Nobori is a thick struts, 2-link design, biolimus-eluting stents.

Outcomes

Primary Outcome Measures

Percentage of uncovered struts

Secondary Outcome Measures

Neointimal thickness
The percentage of malapposed struts
Area of low wall shear stress
Baseline area of low wall shear stress will be calculated within 1 month after obtaining post stent OCT and CTA images.
Area of high oscillatory shear index
Baseline area of high oscillatory shear index will be calculated within 1 month after obtaining post stent OCT and CTA images.
Area of low wall shear stress
Area of high oscillatory shear index

Full Information

First Posted
September 7, 2013
Last Updated
September 10, 2013
Sponsor
Kobe University
Collaborators
Marquette University
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1. Study Identification

Unique Protocol Identification Number
NCT01942044
Brief Title
Relation Among Shear Stress Distribution, Stent Design, and Subsequent Vessel Healing After Drug-eluting Stent Implantation (SHEAR DES)
Official Title
Impact of Stent Platform on Shear Stress Distribution and Subsequent Vessel Healing After Drug-eluting Stent Implantation (SHEAR DES)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2013
Overall Recruitment Status
Unknown status
Study Start Date
February 2013 (undefined)
Primary Completion Date
February 2015 (Anticipated)
Study Completion Date
February 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kobe University
Collaborators
Marquette University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate the differences of wall shear stress distribution among different types of drug-eluting stents and its impact on vessel healing evaluated by intravascular optical coherence tomography evaluation.
Detailed Description
Background: Distribution of wall shear stress (WSS) may be different according to stent designs. The impact of WSS after stent implantation may impact future vessel healing after current generation drug-eluting stents implantation. Although previous studies used IVUS (intravascular ultrasound) and angiography to determine WSS from computational fluid dynamics (CFD) simulations, new methods using higher resolution OCT (optical coherence tomography) are warranted to further evaluate the impact of stent design on WSS with current generation drug-eluting stents. Methods: For these purpose, we will enroll a total of 30 patients with stable angina who are scheduled for percutaneous coronary intervention. Those patients were randomized to thin-strut (81μm) 2-link Promus element (PE: n=10), thin-strut (81μm) 3-link Xience Prime (XP: n=10), or thick-strut (145μm) 2-link Nobori stents (NO: n=10) and underwent OCT and coronary CT angiography (CTA) after stenting. Post stent WSS was calculated using CFD simulations based on patient-specific reconstructed 3D arteries created by the fusion of OCT and CTA data, normalized using WSS in the proximal unstented region. Also, follow-up angiography and OCT are performed for the assessment of vessel healing as well as WSS distribution 8months after stent implantation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Heart Disease
Keywords
Shear stress, Optical coherence tomography, Drug-eluting stents

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Promus element
Arm Type
Experimental
Arm Description
Promus element is a thin struts, 2-link design, evelolimus-eluting stents.
Arm Title
Xience Prime
Arm Type
Active Comparator
Arm Description
Xience Prime is a thin struts, 3-link design, evelolimus-eluting stents.
Arm Title
Nobori
Arm Type
Active Comparator
Arm Description
Nobori is a thick struts, 2-link design, biolimus-eluting stents.
Intervention Type
Device
Intervention Name(s)
Promus element, Xience prime, and Nobori
Primary Outcome Measure Information:
Title
Percentage of uncovered struts
Time Frame
8 months
Secondary Outcome Measure Information:
Title
Neointimal thickness
Time Frame
8 months
Title
The percentage of malapposed struts
Time Frame
8 months
Title
Area of low wall shear stress
Description
Baseline area of low wall shear stress will be calculated within 1 month after obtaining post stent OCT and CTA images.
Time Frame
Baseline
Title
Area of high oscillatory shear index
Description
Baseline area of high oscillatory shear index will be calculated within 1 month after obtaining post stent OCT and CTA images.
Time Frame
Baseline
Title
Area of low wall shear stress
Time Frame
8 months
Title
Area of high oscillatory shear index
Time Frame
8 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Older than 20 years old. Indication of PCI with Xience prime, Nobori, or Promus element. Clinical diagnosis of stable angina, unstable angina or silent ischemia with reference vessel diameters ranging from 2.5-3.5mm. Underwent CT angiography before PCI. To agree to review and record all the clinical course in this research protocol. Exclusion Criteria: Previous history of pancytopenia, liver function, renal dysfunction, hypersensitive history of the drug. Low ejection fraction (LVEF<=30%), an impaired liver function, and renal dysfunction (eGFR<=40) Severe calcification Stent restenosis
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hiromasa Otake, MD, PhD
Phone
+81.78.382.5846
Email
hotake@med.kobe-u.ac.jp
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hiromasa Otake, MD, PhD
Organizational Affiliation
Kobe University Graduate School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kobe University Graduate School of Medicine
City
Kobe
State/Province
Hyogo
ZIP/Postal Code
650-0017
Country
Japan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hiromasa Otake, MD, PhD
Phone
+81.78.382.5846
Email
hotake@med.kobe-u.ac.jp
First Name & Middle Initial & Last Name & Degree
Toshiro Shinke, MD, PhD

12. IPD Sharing Statement

Learn more about this trial

Relation Among Shear Stress Distribution, Stent Design, and Subsequent Vessel Healing After Drug-eluting Stent Implantation (SHEAR DES)

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