RIBS IV (Restenosis Intra-stent of Drug-eluting Stents: Paclitaxel-eluting Balloon vs Everolimus-eluting Stent) (RIBS IV)

RIBS IV (Restenosis Intra-stent of Drug-eluting Stents: Paclitaxel-eluting Balloon vs Everolimus-eluting Stent). A Prospective, Multicenter and Randomized Clinical Trial

Treatment of patients with drug-eluting stent restenosis remains a challenge. This study will assess which interventional strategy (paclitaxel-eluting balloon vs everolimus-eluting stent) is superior in the treatment of patients suffering from drug-eluting stent restenosis.

Study Overview

Detailed Description

Treatment of patients with drug-eluting stent restenosis remains a major clinical and technical challenge. Currently, drug-eluting stents are widely used in the management of these patients. Recently, the value of the paclitaxel-eluting balloon in this clinical setting has been suggested. However, there is only scarce observational data on the value of this new balloon in patients with drug-eluting stent restenosis.

This prospective, multicenter, randomized clinical trial will compare two different interventional strategies (namely, paclitaxel-eluting balloon vs everolimus-eluting stent) in the treatment of patients with drug-eluting stent restenosis.

Study Type

Interventional

Enrollment (Anticipated)

310

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

      • A Coruña, Spain, 15006
        • Recruiting
        • Complejo Hospitalario Universitario A Coruña
        • Contact:
          • Nicolas Vazquez, MD
          • Phone Number: 0034981178031
        • Principal Investigator:
          • Nicolas Vazquez, MD
      • Alicante, Spain, 03010
        • Recruiting
        • Hospital General Universitario de Alicante
        • Contact:
          • Vicente Mainar, MD
          • Phone Number: 0034965938561
        • Principal Investigator:
          • Vicente Mainar, MD
      • Almeria, Spain, 04009
        • Recruiting
        • Complejo Hospitalario de Torrecardenas
        • Contact:
          • Rosa Lazaro, MD,
          • Phone Number: +34950016989
        • Principal Investigator:
          • Rosa Lazaro, MD
      • Badajoz, Spain, 06080
        • Recruiting
        • Hospital Universitario Infanta Cristina
        • Contact:
          • Jose R Lopez-Minguez, MD
          • Phone Number: 0034924218125
        • Principal Investigator:
          • Jose R Lopez-Minguez, MD
      • Barcelona, Spain, 08036
        • Recruiting
        • Hospital Clinic de Barcelona
        • Contact:
          • Monica Masotti, MD
          • Phone Number: 0034932275519
        • Principal Investigator:
          • Monica Masotti, MD
      • Barcelona, Spain, 08025
        • Recruiting
        • Hospital de la Santa Creu i Sant Pau
        • Contact:
          • Vicens Marti, MD
          • Phone Number: 0034935565851
        • Principal Investigator:
          • Vicens Marti, MD
      • Barcelona, Spain, 08035
        • Recruiting
        • Hospital Universitari Vall d´Hebron
        • Contact:
          • Joan Angel, MD
          • Phone Number: 0034934893000
        • Principal Investigator:
          • Joan Angel, MD
      • Granada, Spain, 18014
        • Recruiting
        • Hospital Universitario Virgen de Las Nieves
        • Contact:
          • Rafael Melgares, MD
          • Phone Number: 0034958020564
        • Principal Investigator:
          • Rafael Melgares, MD
      • Madrid, Spain, 28041
        • Recruiting
        • Hospital Universitario 12 de Octubre
        • Contact:
          • Maria T Velazquez, MD
          • Phone Number: 0034913908440
        • Principal Investigator:
          • Maria T Velazquez, MD
      • Madrid, Spain, 28046
        • Recruiting
        • Hospital Universitario La Paz
        • Contact:
          • Raul Moreno, MD
          • Phone Number: 0034917277000
        • Principal Investigator:
          • Raul Moreno, MD
      • Madrid, Spain, 28040
        • Recruiting
        • Hospital Clinico San Carlos
        • Contact:
        • Principal Investigator:
          • Fernando Alfonso, MD, PhD
      • Madrid, Spain, 28006
        • Recruiting
        • Hospital Universitario de La Princesa
        • Contact:
          • Bernhard Seidelberger, MD
          • Phone Number: 0034915202200
        • Principal Investigator:
          • Bernhard Seidelberger, MD
      • Malaga, Spain, 29010
        • Recruiting
        • Hospital Universitario Virgen de la Victoria
        • Contact:
          • Jose M Hernandez, MD
          • Phone Number: 0034951032000
        • Principal Investigator:
          • Jose M Hernandez, MD
      • Malaga, Spain, 29010
        • Recruiting
        • Hospital Universitario Carlos Haya
        • Contact:
          • Cristobal Urbano, MD
          • Phone Number: 0034951290000
        • Principal Investigator:
          • Cristobal Urbano, MD
      • Toledo, Spain, 45004
        • Recruiting
        • Complejo Hospitalario de Toledo
        • Contact:
          • Jose Moreu, MD
          • Phone Number: +34925269188
        • Principal Investigator:
          • Jose Moreu, MD
      • Valencia, Spain, 46010
        • Recruiting
        • Hospital Clinico Universitario de Valencia
        • Contact:
          • Vicent Bodi, MD
          • Phone Number: 0034963862658
        • Principal Investigator:
          • Vicent Bodi, MD
      • Valencia, Spain, 46014
        • Recruiting
        • Hospital General Universitario de Valencia
        • Contact:
          • Francisco Pomar, MD
          • Phone Number: 0034961972000
        • Principal Investigator:
          • Francisco Pomar, MD
      • Zaragoza, Spain, 50009
        • Recruiting
        • Hospital Universitario Miguel Servet
        • Contact:
          • Maria Cruz Ferrer, MD, PhD
          • Phone Number: +34976562565
        • Principal Investigator:
          • Maria Cruz Ferrer, MD, PhD
    • Asturias
      • Oviedo, Asturias, Spain, 33006
        • Recruiting
        • Hospital Central de Asturias
        • Contact:
          • Raquel del Valle, MD
          • Phone Number: 0034985106112
        • Principal Investigator:
          • Raquel del Valle, MD
    • Barcelona
      • L´Hospitalet de Llobregat, Barcelona, Spain, 08907
        • Recruiting
        • Hospital Universitari de Bellvitge
        • Contact:
          • Angel Cequier, MD
          • Phone Number: 0034932607539
        • Principal Investigator:
          • Angel Cequier, MD
    • Cantabria
      • Santander, Cantabria, Spain, 39008
        • Recruiting
        • Hospital Universitario Marques de Valdecilla
        • Contact:
          • Javier Zueco, MD
          • Phone Number: 0034942202744
        • Principal Investigator:
          • Javier Zueco, MD
    • Illes Balears
      • Palma de Mallorca, Illes Balears, Spain, 07014
        • Recruiting
        • Hospital Universitari Son Dureta
        • Contact:
          • Armando Bethencourt, MD
          • Phone Number: 0034971175476
        • Principal Investigator:
          • Armando Bethencourt, MD
    • Madrid
      • Majadahonda, Madrid, Spain, 28222
        • Recruiting
        • Hospital Universitario Puerta de Hierro Majadahonda
        • Contact:
          • Javier Goicolea, MD
          • Phone Number: 0034911917408
        • Principal Investigator:
          • Javier Goicolea, MD
    • Navarra
      • Pamplona, Navarra, Spain, 31008
        • Recruiting
        • Hospital Provincial de Navarra
        • Contact:
          • Roman Lezaun, MD
          • Phone Number: 0034848422345
        • Principal Investigator:
          • Roman Lezaun, MD
    • Pontevedra
      • Vigo, Pontevedra, Spain, 36200
        • Recruiting
        • Complejo Hospitalario Universitario de Vigo
        • Contact:
          • Andres Iñiguez, MD
          • Phone Number: 0034986811163
        • Principal Investigator:
          • Andres Iñiguez, MD

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

Inclusion Criteria:

PATIENT:

  • Age between 20 and 85 years
  • Signed informed consent
  • Acceptance of late angiographic control (6-9 months)
  • Angina and / or objective evidence of ischemia

LESION:

  • In-Stent restenosis (> 50% visual) any drug-eluting stent
  • Knowledge of prior stent location

Exclusion Criteria:

PATIENT:

  • Inclusion in another clinical research protocol
  • Women of childbearing age
  • Severe associated systemic disease (including renal or liver failure)
  • Severe depression of left ventricular ejection fraction (LVEF <25%)
  • Disease that affects life expectancy
  • Recent myocardial infarction ( <7 days)
  • Time of implantation of the previous DES <1 month
  • Severe difficulties expected for late angiographic study

LESION:

  • Angiographic failure during implementation of initial stent(residual stenosis> 50%)
  • Image of large thrombus in-stent (> vessel diameter)
  • Tortuosity or Ca + + with very severe difficulties during prior stent deployment
  • Vessel diameter <2 mm (visual estimate)
  • Restenosis only "outside" the stent (The edge of the stent is not affected)
  • Completely occlusive restenosis (100%, TIMI 0)
  • Very diffuse restenosis (> 30 mm 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: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Paclitaxel-eluting balloon
Paclitaxel-eluting balloon (SeQuent Please, B. Braun)
Balloon angioplasty
Active Comparator: Everolimus-eluting stent
Everolimus-eluting stent (Xience Prime, Abbott Vascular)
Stent implantation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Minimal lumen diameter
Time Frame: Late angiographic follow-up (6-9 months)
Comparison of minimal lumen diameter at late angiographic follow-up (6-9 months) between the 2 treatment strategies (by quantitative coronary angiography)
Late angiographic follow-up (6-9 months)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Combined clinical and angiographic end-points
Time Frame: 6-9 months, 1 year and 3 years

A) Efficacy outcomes:

A1) Angiographic: 1) Restenosis rate, 2) % diameter stenosis, 3) acute gain, 4) late loss, 5) net gain A2) Composite of death, myocardial infarction, target vessel revascularization and analysis of individual events

B) Safety Outcomes: Stent thrombosis, Bleeding episodes.

C) Pre-specified variables for subgroup analysis (RIBS I)

D) Stratification (length and edge). Type of stent and eluted drug

E) Influence of clinical variables and restenosis patterns on outcome

6-9 months, 1 year and 3 years

Collaborators and Investigators

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

Investigators

  • Study Director: Fernando Alfonso, MD, PhD, Hospital San Carlos, Madrid

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

January 1, 2010

Primary Completion (Anticipated)

July 1, 2012

Study Registration Dates

First Submitted

November 12, 2010

First Submitted That Met QC Criteria

November 12, 2010

First Posted (Estimate)

November 15, 2010

Study Record Updates

Last Update Posted (Estimate)

June 27, 2011

Last Update Submitted That Met QC Criteria

June 23, 2011

Last Verified

November 1, 2010

More Information

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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