Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment (RIBS VI) (RIBS VI)

February 20, 2017 updated by: Fernando Alfonso, Spanish Society of Cardiology

Prospective Study of Bioresorbable Vascular Scaffold Treatment in Patients With In-stent Restenosis

Treatment of patients with in-stent restenosis (ISR) remains a challenge. This study will assess the efficacy of Bioresorbable Vascular Scaffolds (BVS) (Abbott Vascular) in the treatment of patients suffering from ISR.

Study Overview

Status

Unknown

Detailed Description

Treatment of patients with ISR remains a challenge. Currently both drug-eluting stents (DES) and drug-coated balloons (DCB) are considered as the strategies of choice in this setting. However, data on the value of BVS in patients with ISR is scarce. BVS are very effective to inhibit neointimal proliferation and they avoid the need of implanting a new permanent metal layer. Accordingly, currently, there is a major interest to elucidate the potential value of BVS in patients with ISR.

This prospective Spanish multicenter study will assess the clinical and angiographic outcome of patients with ISR treated with BVS. BVS will be implanted in selected patients (fulfilling inclusion and exclusion criteria) presenting with either BMS-ISR or DES-ISR. Care will be paid to ensure device optimization. Angiographic follow-up will be obtained at 6-9 months. A centralized angiographic corelab will be used to provide QCA measurements. Clinical follow-up will be also obtained at 1 year and then yearly. Clinical events will be adjudicated by an independent Clinical Event Committee.

Study Type

Interventional

Enrollment (Anticipated)

130

Phase

  • Phase 4

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Badajoz, Spain, 06080
        • Hospital Universitario Infanta Cristina
      • Barcelona, Spain, 08036
        • Hospital Clinic de Barcelona
      • Barcelona, Spain, 08025
        • Hospital de la Santa Creu i Sant Pau
      • Barcelona, Spain, 08035
        • Hospital Universitari Vall d´Hebrón
      • Granada, Spain, 18014
        • Hospital Universitario Virgen de las Nieves
      • León, Spain, 24071
        • Complejo Asistencial de León
      • Madrid, Spain, 28041
        • Hospital Universitario 12 de Octubre
      • Madrid, Spain, 28046
        • Hospital Universitario La Paz
      • Madrid, Spain, 28006
        • Hospital Universitario de la Princesa
      • Madrid, Spain, 28034
        • Hospital Ramon y Cajal
      • Toledo, Spain, 45004
        • Complejo Hospitalario de Toledo
      • Valladolid, Spain, 47005
        • Hospital Clinico Universitario de Valladolid
      • Vizcaya, Spain, 48960
        • Hospital de Galdakao
    • A Coruña
      • Santiago de Compostela, A Coruña, Spain, 15006
        • Complexo Universitario Hospitalario de Santiago
    • Asturias
      • Oviedo, Asturias, Spain, 33006
        • Hospital Central de Asturias
    • Barcelona
      • L´Hospitalet de Llobregat, Barcelona, Spain, 08907
        • Hospital Universitari de Bellvitge
    • Cantabria
      • Santander, Cantabria, Spain, 39008
        • Hospital Universitario Marqués de Valdecilla
    • Madrid
      • Majadahonda, Madrid, Spain, 28222
        • Hospital Universitario Puerta de Hierro
    • Santa Cruz de Tenerife
      • San Cristobal de La Laguna, Santa Cruz de Tenerife, Spain, 38320
        • Hospital Universitario de Canarias

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 85 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

In-stent restenosis with ischemia. Signed Informed Consent IRB approval

INCLUSION CRITERIA:

PATIENT

  • Age > 20 and < 85 years of age
  • Acceptance of late angiographic evaluation
  • Angina or objective evidence of ischemia

LESION

  • ISR (>50% diameter stenosis on visual assessment)
  • Previous stent location known

EXCLUSION CRITERIA:

PATIENT

  • Inclusion in other clinical research protocol
  • Allergy to antiplatelet agents
  • Women in childbearing age
  • Severe associated systemic diseases (including renal or liver failure) or diseases affecting life expectancy
  • Recent myocardial infarction
  • Time from index stent implantation < 1 month
  • Anticipated difficulties for late angiographic evaluation

LESION

  • Stent thrombosis or large thrombus within the stent
  • Angiographic failure during initial stent implantation or persistence or large dissection.
  • Severe tortuosity or calcification or major difficulties during previous stent implantation
  • Vessel diameter < 2.25 mm (visual assessment)
  • Stenosis outside stent stent edge (edge ISR are eligible)
  • Very diffuse ISR (>30 mm in length)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: NA
  • Interventional Model: SINGLE_GROUP
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: BVS implantation in patients with ISR

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Minimal lumen diameter as assessed by quantitative coronary angiography at late angiographic follow-up
Time Frame: angiographic follow-up at 6-9 months
This is a single arm study and results will be analyzed per arm. However, the angiographic and clinical results will be also compared with those obtained in other arms of previous RIBS trials
angiographic follow-up at 6-9 months
Combined clinical end-point (cardiac death, myocardial infarction and target vessel revascularization)
Time Frame: 1 year of clinical follow-up
This is a well-accepted outcome measure of individual clinical end-points. Definition of myocardial infarction is similar to that used in previous RIBS studies.
1 year of clinical follow-up

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cardiac death
Time Frame: 1 year, 2 years, 3 years, 4 years, 5 years
Individual clinical outcome
1 year, 2 years, 3 years, 4 years, 5 years
Total mortality
Time Frame: 1 year, 2 years, 3 years, 4 years, 5 years
Individual clinical outcome
1 year, 2 years, 3 years, 4 years, 5 years
Myocardial infarction
Time Frame: 1 year, 2 years, 3 years, 4 years, 5 years
Individual clinical outcome
1 year, 2 years, 3 years, 4 years, 5 years
Target vessel revascularization
Time Frame: 1 year, 2 years, 3 years, 4 years, 5 years
Individual clinical outcome
1 year, 2 years, 3 years, 4 years, 5 years
Target lesion revascularization
Time Frame: 1 year, 2 years, 3 years, 4 years, 5 years
Individual clinical outcome
1 year, 2 years, 3 years, 4 years, 5 years
Stent thrombosis
Time Frame: 1 year, 2 years, 3 years, 4 years, 5 years
Individual clinical outcome
1 year, 2 years, 3 years, 4 years, 5 years
Major bleeding
Time Frame: 1 year, 2 years, 3 years, 4 years, 5 years
Individual clinical outcome
1 year, 2 years, 3 years, 4 years, 5 years
Acute gain
Time Frame: procedure
Change in the minimal lumen diameter from baseline to the final procedural angiogram. Acute angiographic parameter.
procedure
Minimal lumen diameter
Time Frame: procedure
Acute angiographic parameter
procedure
Percent diameter stenosis
Time Frame: procedure
Acute angiographic parameter
procedure
Restenosis rate
Time Frame: 6-9 months
Late angiographic parameter
6-9 months
Percent diameter stenosis
Time Frame: 6-9 months
Late angiographic parameter
6-9 months
Late loss
Time Frame: 6-9 months
Change in minimal lumen diameter from the final procedure to the follow-up angiogram at 6-9 months. Late angiographic parameter.
6-9 months
Net gain
Time Frame: 6-9 months
Is the difference between acute gain and late loss. Late angiographic parameter.
6-9 months
Loss index
Time Frame: 6-9 months
Late angiographic parameter
6-9 months
Combined clinical outcome measure (Cardiac death, Myocardial infarction, target lesion revascularization)
Time Frame: 1 year, 2 years, 3 years, 4 years, 5 years
This is a well-accepted outcome measure of individual clinical end-points. Definition of myocardial infarction is similar to that used in previous RIBS studies.
1 year, 2 years, 3 years, 4 years, 5 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

April 1, 2014

Primary Completion (ACTUAL)

December 1, 2016

Study Completion (ANTICIPATED)

December 1, 2020

Study Registration Dates

First Submitted

January 5, 2016

First Submitted That Met QC Criteria

February 2, 2016

First Posted (ESTIMATE)

February 3, 2016

Study Record Updates

Last Update Posted (ACTUAL)

February 23, 2017

Last Update Submitted That Met QC Criteria

February 20, 2017

Last Verified

February 1, 2017

More Information

Terms related to this study

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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