Cargando…

Rationale and Design of Randomized Clinical Trial for the Assessment of Macitentan Efficiency as Coadjuvant Treatment to Open and Endovascular Revascularization in Critical Limb Ischemia

INTRODUCTION: Critical limb ischemia (CLI) is defined by ischemic rest pain, tissue loss, or both, secondary to arterial insufficiency, and its prevalence is increasing mainly as a result of the worldwide high prevalence of diabetes. Currently, there are no available conclusive data on the efficacy...

Descripción completa

Detalles Bibliográficos
Autores principales: Michel, Ignacio, De Haro, Joaquin, Bleda, Silvia, Laime, Ilsem V., Uyaguari, Jhenifer, Acin, Francisco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096766/
https://www.ncbi.nlm.nih.gov/pubmed/27840580
http://dx.doi.org/10.4137/CMC.S38448
_version_ 1782465522051317760
author Michel, Ignacio
De Haro, Joaquin
Bleda, Silvia
Laime, Ilsem V.
Uyaguari, Jhenifer
Acin, Francisco
author_facet Michel, Ignacio
De Haro, Joaquin
Bleda, Silvia
Laime, Ilsem V.
Uyaguari, Jhenifer
Acin, Francisco
author_sort Michel, Ignacio
collection PubMed
description INTRODUCTION: Critical limb ischemia (CLI) is defined by ischemic rest pain, tissue loss, or both, secondary to arterial insufficiency, and its prevalence is increasing mainly as a result of the worldwide high prevalence of diabetes. Currently, there are no available conclusive data on the efficacy of any coadjuvant therapy after revascularization procedure benefiting amputation and patency rates. Macitentan is an orally active dual endothelin (ET) receptor antagonist that may contribute to reduce the amputation rate and improve revascularization patency in CLI. METHODS/DESIGN: REVASC is a proposed pilot, open-label, controlled, randomized, single-center clinical double-blind trial to be conducted in Spain on a study population of European patients with CLI, which will compare the clinical outcomes and cost-effectiveness of macitentan coadjuvant treatment after limb revascularization with the standard antiplatelet treatment strategy for severe limb ischemia. Patients are randomized 1:1 to receive macitentan or placebo for 12 weeks. The primary clinical end point will be amputation-free survival rate at 12 months, defined as the time to major (above the ankle) amputation for the index (trial) limb or death from any cause, whichever comes first. Secondary outcomes include overall survival, quality of life, in-hospital mortality and morbidity, repeat interventions, healing of tissue loss, and hemodynamic changes following revascularization. Sample size is estimated as 120 patients. The economic analysis will consist of two components: a “within-study” analysis, which will be based on study end points; and a “model-based” analysis, which will extrapolate and compare costs and effects likely to accrue beyond the study follow-up period. DISCUSSION: The REVASC trial is designed to be pragmatic and represents current practice of the real-world population management after limb revascularization for CLI due to atherosclerosis. Current evidence does not support any coadjuvant treatment. A new pathway of treatment may be opened with the use of ET receptor antagonists in these patients.
format Online
Article
Text
id pubmed-5096766
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Libertas Academica
record_format MEDLINE/PubMed
spelling pubmed-50967662016-11-12 Rationale and Design of Randomized Clinical Trial for the Assessment of Macitentan Efficiency as Coadjuvant Treatment to Open and Endovascular Revascularization in Critical Limb Ischemia Michel, Ignacio De Haro, Joaquin Bleda, Silvia Laime, Ilsem V. Uyaguari, Jhenifer Acin, Francisco Clin Med Insights Cardiol Research Proposal INTRODUCTION: Critical limb ischemia (CLI) is defined by ischemic rest pain, tissue loss, or both, secondary to arterial insufficiency, and its prevalence is increasing mainly as a result of the worldwide high prevalence of diabetes. Currently, there are no available conclusive data on the efficacy of any coadjuvant therapy after revascularization procedure benefiting amputation and patency rates. Macitentan is an orally active dual endothelin (ET) receptor antagonist that may contribute to reduce the amputation rate and improve revascularization patency in CLI. METHODS/DESIGN: REVASC is a proposed pilot, open-label, controlled, randomized, single-center clinical double-blind trial to be conducted in Spain on a study population of European patients with CLI, which will compare the clinical outcomes and cost-effectiveness of macitentan coadjuvant treatment after limb revascularization with the standard antiplatelet treatment strategy for severe limb ischemia. Patients are randomized 1:1 to receive macitentan or placebo for 12 weeks. The primary clinical end point will be amputation-free survival rate at 12 months, defined as the time to major (above the ankle) amputation for the index (trial) limb or death from any cause, whichever comes first. Secondary outcomes include overall survival, quality of life, in-hospital mortality and morbidity, repeat interventions, healing of tissue loss, and hemodynamic changes following revascularization. Sample size is estimated as 120 patients. The economic analysis will consist of two components: a “within-study” analysis, which will be based on study end points; and a “model-based” analysis, which will extrapolate and compare costs and effects likely to accrue beyond the study follow-up period. DISCUSSION: The REVASC trial is designed to be pragmatic and represents current practice of the real-world population management after limb revascularization for CLI due to atherosclerosis. Current evidence does not support any coadjuvant treatment. A new pathway of treatment may be opened with the use of ET receptor antagonists in these patients. Libertas Academica 2016-11-03 /pmc/articles/PMC5096766/ /pubmed/27840580 http://dx.doi.org/10.4137/CMC.S38448 Text en © 2016 the author(s), publisher and licensee Libertas Academica Ltd. This is an open-access article distributed under the terms of the Creative Commons CC-BY-NC 3.0 License.
spellingShingle Research Proposal
Michel, Ignacio
De Haro, Joaquin
Bleda, Silvia
Laime, Ilsem V.
Uyaguari, Jhenifer
Acin, Francisco
Rationale and Design of Randomized Clinical Trial for the Assessment of Macitentan Efficiency as Coadjuvant Treatment to Open and Endovascular Revascularization in Critical Limb Ischemia
title Rationale and Design of Randomized Clinical Trial for the Assessment of Macitentan Efficiency as Coadjuvant Treatment to Open and Endovascular Revascularization in Critical Limb Ischemia
title_full Rationale and Design of Randomized Clinical Trial for the Assessment of Macitentan Efficiency as Coadjuvant Treatment to Open and Endovascular Revascularization in Critical Limb Ischemia
title_fullStr Rationale and Design of Randomized Clinical Trial for the Assessment of Macitentan Efficiency as Coadjuvant Treatment to Open and Endovascular Revascularization in Critical Limb Ischemia
title_full_unstemmed Rationale and Design of Randomized Clinical Trial for the Assessment of Macitentan Efficiency as Coadjuvant Treatment to Open and Endovascular Revascularization in Critical Limb Ischemia
title_short Rationale and Design of Randomized Clinical Trial for the Assessment of Macitentan Efficiency as Coadjuvant Treatment to Open and Endovascular Revascularization in Critical Limb Ischemia
title_sort rationale and design of randomized clinical trial for the assessment of macitentan efficiency as coadjuvant treatment to open and endovascular revascularization in critical limb ischemia
topic Research Proposal
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096766/
https://www.ncbi.nlm.nih.gov/pubmed/27840580
http://dx.doi.org/10.4137/CMC.S38448
work_keys_str_mv AT michelignacio rationaleanddesignofrandomizedclinicaltrialfortheassessmentofmacitentanefficiencyascoadjuvanttreatmenttoopenandendovascularrevascularizationincriticallimbischemia
AT deharojoaquin rationaleanddesignofrandomizedclinicaltrialfortheassessmentofmacitentanefficiencyascoadjuvanttreatmenttoopenandendovascularrevascularizationincriticallimbischemia
AT bledasilvia rationaleanddesignofrandomizedclinicaltrialfortheassessmentofmacitentanefficiencyascoadjuvanttreatmenttoopenandendovascularrevascularizationincriticallimbischemia
AT laimeilsemv rationaleanddesignofrandomizedclinicaltrialfortheassessmentofmacitentanefficiencyascoadjuvanttreatmenttoopenandendovascularrevascularizationincriticallimbischemia
AT uyaguarijhenifer rationaleanddesignofrandomizedclinicaltrialfortheassessmentofmacitentanefficiencyascoadjuvanttreatmenttoopenandendovascularrevascularizationincriticallimbischemia
AT acinfrancisco rationaleanddesignofrandomizedclinicaltrialfortheassessmentofmacitentanefficiencyascoadjuvanttreatmenttoopenandendovascularrevascularizationincriticallimbischemia