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Comparison of the Vasomotor Function and Myocardial Flow in Patients Treated With Bioresorbable and Metallic Stents at 1 Year (BVS-Flow)

Primary Purpose

Stable Angina

Status
Completed
Phase
Phase 4
Locations
Spain
Study Type
Interventional
Intervention
Bioresorbable vascular scaffold
Everolimus-eluting stent
Sponsored by
Institut d'Investigació Biomèdica de Bellvitge
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Stable Angina focused on measuring Coronary microcirculatory dysfunction, Coronary endothelium dysfunction

Eligibility Criteria

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

Inclusion Criteria:

  • Patients with stable angina or silent angina with myocardial ischemia detected by non-invasive tests or patients with acute coronary syndromes with no increase of > 5 times the upper value of normality of cardiac biomarkers (troponin).
  • Patients with coronary artery disease with angiographic stenosis >

Sites / Locations

  • Hospital Universitari de Bellvitge
  • Hospital del Mar
  • Hospital Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Bioresorbable vascular scaffold (BVS)

Everolimus-eluting stent (EES)

Arm Description

Patients with stable coronary angina with coronary artery disease suitable to be treated with a bioresorbable vascular scaffold.

Patients with stable coronary angina with coronary artery disease suitable to be treated with a Everolimus-eluting stent .

Outcomes

Primary Outcome Measures

Difference in the average peak velocity at maximal hyperemia between bioresorbable vascular scaffolds and everolimus-eluting stents as assessed by doppler wire measurement.

Secondary Outcome Measures

Difference in endothelial dysfunction with acetyl-choline infusion between bioresorbable vascular scaffolds and everolimus-eluting stents as assessed by quantitative coronary angiography (4% of lumen reduction)

Full Information

First Posted
April 11, 2016
Last Updated
July 2, 2018
Sponsor
Institut d'Investigació Biomèdica de Bellvitge
Collaborators
Fundació La Marató de TV3
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1. Study Identification

Unique Protocol Identification Number
NCT02738658
Brief Title
Comparison of the Vasomotor Function and Myocardial Flow in Patients Treated With Bioresorbable and Metallic Stents at 1 Year
Acronym
BVS-Flow
Official Title
Comparison of the Vasomotor Function and Myocardial Flow in Patients Treated
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
March 1, 2015 (Actual)
Primary Completion Date
July 2, 2018 (Actual)
Study Completion Date
July 2, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Institut d'Investigació Biomèdica de Bellvitge
Collaborators
Fundació La Marató de TV3

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Background: A total of 25-50% of patients with stable coronary atherosclerosis treated with metallic stent implantation remain with effort angina despite optimal medical treatment and absence of stent restenosis at 1 year. The most plausible cause of persistent effort angina after stent implantation is microcirculatory dysfunction. Coronary circulation matches the myocardial blood supply and oxygen consumption. Metallic stent implantation has been related with endothelial dysfunction and impaired coronary blood flow reserve (relation between coronary blood flow at rest and maximal hyperemia) of the treated vessel at 1 year. Bioresorbable Vascular Scaffold (BVS) has been shown to improve the endothelial function and to improve the angina symptoms at 1 year. However, the coronary blood flow of BVS has never been tested. Main objective: To determine differences in the blood average peak velocity at maximal hyperemia with adenosine infusion between patients treated with bioresorbable and metallic coronary stents at 1 year after stent implantation. Methodology: A total of 70 patients are 1:1 randomized to everolimus-eluting metallic stent (EES) versus everolimus-eluting BVS implantation in patients with stable coronary disease. At 1 year, patients undergo to invasive coronary angiography prior cessation of vasomotor drugs. A pressure/Doppler wire is advanced distally to the "treated segment" and the endothelial (acetylcholine) and non-endothelial (adenosine and nitroglycerine) vasomotor function is assessed with quantitative coronary angiography and pressure and Doppler measurements. Angina test questionnaires are obtained at different time-points of the study. Expected results: A difference between patients treated with BVS and EES of 12.0 cm/sc in the maximal average peak velocity (APV) under maximal hyperemia (with adenosine administration) is expected, as assessed by Doppler measurements, at 1 year after stent implantation. The study is powered to assess superiority in terms of maximal APV favoring patients treated with BVS.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stable Angina
Keywords
Coronary microcirculatory dysfunction, Coronary endothelium dysfunction

7. Study Design

Primary Purpose
Other
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
70 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Bioresorbable vascular scaffold (BVS)
Arm Type
Experimental
Arm Description
Patients with stable coronary angina with coronary artery disease suitable to be treated with a bioresorbable vascular scaffold.
Arm Title
Everolimus-eluting stent (EES)
Arm Type
Active Comparator
Arm Description
Patients with stable coronary angina with coronary artery disease suitable to be treated with a Everolimus-eluting stent .
Intervention Type
Device
Intervention Name(s)
Bioresorbable vascular scaffold
Other Intervention Name(s)
Bioresorbable stents
Intervention Type
Device
Intervention Name(s)
Everolimus-eluting stent
Primary Outcome Measure Information:
Title
Difference in the average peak velocity at maximal hyperemia between bioresorbable vascular scaffolds and everolimus-eluting stents as assessed by doppler wire measurement.
Time Frame
1-year after stent implantation
Secondary Outcome Measure Information:
Title
Difference in endothelial dysfunction with acetyl-choline infusion between bioresorbable vascular scaffolds and everolimus-eluting stents as assessed by quantitative coronary angiography (4% of lumen reduction)
Time Frame
1-year after stent implantation
Other Pre-specified Outcome Measures:
Title
Difference in fractional flow reserve at maximal hyperemia between the two treatment groups as assessed by pressure-wire measurement
Time Frame
1-year after stent implantation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with stable angina or silent angina with myocardial ischemia detected by non-invasive tests or patients with acute coronary syndromes with no increase of > 5 times the upper value of normality of cardiac biomarkers (troponin). Patients with coronary artery disease with angiographic stenosis >
Facility Information:
Facility Name
Hospital Universitari de Bellvitge
City
L´Hospitalet de Llobregat
State/Province
Barcelona
ZIP/Postal Code
08173
Country
Spain
Facility Name
Hospital del Mar
City
Barcelona
ZIP/Postal Code
08003
Country
Spain
Facility Name
Hospital Clinic
City
Barcelona
ZIP/Postal Code
08036
Country
Spain

12. IPD Sharing Statement

Learn more about this trial

Comparison of the Vasomotor Function and Myocardial Flow in Patients Treated With Bioresorbable and Metallic Stents at 1 Year

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