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Hybrid Revascularization Observational Study

7 febbraio 2014 aggiornato da: Icahn School of Medicine at Mount Sinai
The purpose of the study is to get a better understanding of patients who have multi-vessel coronary artery disease (blockages in more than one vessel bringing blood to the heart) and have either Hybrid Coronary Revascularization [HCR] (combination of surgery and catheter procedures to open up clogged heart arteries) or Percutaneous Coronary Intervention [PCI] (catheter procedures to open up clogged heart arteries). Participation in the study will last up to 21 months after a patient's heart procedure(s). The study collects information about the medical care patients receive during their planned procedure(s) and how well they do following the procedure(s). No new testing or procedures will be done. Patients will receive only the tests or procedures their doctor already has planned for them. The information collected should help to plan the design of a pivotal comparative effectiveness study of hybrid revascularization.

Panoramica dello studio

Stato

Completato

Descrizione dettagliata

The increasing prevalence of coronary artery disease (CAD), advances in coronary artery bypass grafting (CABG), percutaneous coronary intervention (PCI), and concomitant medical therapy, and the costs of revascularization have resulted in rising interest regarding the appropriate indications for coronary revascularization. For patients with 3-vessel disease, revascularization by CABG has recently been rated as appropriate while revascularization by PCI has been rated uncertain. Ideally, physicians would like to offer their multi-vessel CAD patients what they truly seek: a solution which provides a safe, minimally invasive treatment that does not compromise long term durability and survival. Integrating the positive features of both PCI and CABG has been the fundamental rationale of "hybrid" coronary revascularization.

Hybrid Coronary Revascularization (HCR) (the intended combination of CABG and PCI) as a scientifically validated approach would have a major healthcare impact. The ability to deliver a new therapy for CAD that provides durability, but without the obligatory trauma and prolonged recovery time characteristic of conventional CABG would be a major advance in the field of cardiovascular medicine. Candidates in whom HCR would be particularly advantageous would be several subgroups of CAD patients that are increasing in numbers: the elderly, patients with a high predicted risk of mortality and/or morbidity for CABG, deconditioned patients or patients with significant disabilities and patients in whom treatment durability is important, but a significantly invasive approach is not an option. Moreover, HCR is likely to bridge the divide in treatment philosophies and approaches that exist between cardiologists and cardiac surgeons. Collaboration rather than competition between these specialties will ultimately benefit patients, hospitals, payers and healthcare providers. The Hybrid Revascularization Observational Study is a multi-center observational study planning grant which will explore target populations for Hybrid Coronary Revascularization (HCR), their outcomes, and variations in specific ways these patients are managed, in order to inform the design of a pivotal comparative effectiveness trial of this emerging therapeutic strategy.

Given the observational nature of the study, the HCR and PCI groups' baseline characteristics and event rates are not directly comparable; rather, the results were intended to inform the design of a larger, randomized pivotal trial. The study was designed in two phases: Cohort 1, which captured demographic, angiographic, and practice patterns data for 6,669 consecutively screened patients; and Cohort 2 which captured demographic, angiographic, practice patterns, and outcome data for 298 patients who underwent either HCR or PCI with DES (90 of whom were also part of Cohort 1).

Tipo di studio

Osservativo

Iscrizione (Effettivo)

298

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Georgia
      • Atlanta, Georgia, Stati Uniti, 30308
        • Emory University
    • Maryland
      • Baltimore, Maryland, Stati Uniti, 21201
        • University of Maryland
    • Massachusetts
      • Boston, Massachusetts, Stati Uniti, 02115
        • Brigham & Women's Hospital
    • New York
      • Bronx, New York, Stati Uniti, 10461
        • Montefiore Medical Center
      • New York, New York, Stati Uniti, 10032
        • Columbia University Medical Center
    • North Carolina
      • Durham, North Carolina, Stati Uniti, 27710
        • Duke University Medical Center
    • Ohio
      • Columbus, Ohio, Stati Uniti, 43210
        • Ohio State University
    • Pennsylvania
      • Philadelphia, Pennsylvania, Stati Uniti, 19104
        • University of Pennsylvania
      • Wynnewood, Pennsylvania, Stati Uniti, 19096
        • Lankenau Hospital
    • Tennessee
      • Nashville, Tennessee, Stati Uniti, 37232
        • Vanderbilt University
    • Virginia
      • Charlottesville, Virginia, Stati Uniti, 22908
        • University of Virginia Health Systems

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

Cohort 1 (Angiogram Review Group): All consecutive and consenting patients undergoing diagnostic cardiac catheterization in a 3 month period.

Cohort 2 (Therapeutic Intervention Group): All patients (including those from cohort 1) who meet either of the following: (a) undergo HCR with minimally invasive LIMA-LAD CABG (HCR Group) OR (b) meet the proposed anatomic and clinical eligibility criteria defined below and undergo multivessel PCI with DES (PCI Group).

Descrizione

The following criteria apply to Cohort 2 PCI patients only:

Inclusion Criteria:

  • Signed informed consent, release of medical information, and Health Insurance Portability and Accountability Act (HIPAA) documents
  • Age 18 years or older
  • Clinical indication for revascularization
  • LAD and at least one additional vessel coronary disease (> 70% stenosis) confirmed by angiogram
  • Clinical characteristics and multi-vessel disease amenable to both PCI with DES and Hybrid as adjudicated by one interventional cardiologist and one cardiac surgeon
  • Ability to tolerate and no plans to interrupt double platelet therapy for ≥ 12 months
  • Ability to tolerate to single lung ventilation in the judgment of the investigator
  • Willing to comply with all protocol required follow-up

Exclusion Criteria:

  • Previous coronary stent within:

    • 1 month prior to enrollment for bare metal stent (BMS) or
    • 6 months prior to enrollment for DES
  • Evidence of in stent restenosis of a DES or BMS
  • Previous cardiac surgery of any kind
  • Chronic total occlusion (CTO) in LAD or ≥ 2 CTOs in major coronary territories that are considered targets for revascularization
  • Left main disease ≥ 50% stenosis
  • Presence of fresh coronary thrombus
  • Need for concomitant vascular or other cardiac surgery during the index hospitalization (including, but not limited to, valve surgery, aortic resection, left ventricular aneurysm, carotid endarterectomy or stenting, etc)
  • Previous STEMI within 30 days prior to randomization
  • Previous stroke within 6 months prior to randomization
  • Previous thoracic surgery involving the left pleural space
  • Acute decompensated heart failure within 30 days prior to randomization
  • Ejection fraction < 30%
  • Creatinine clearance ≤ 50 ml/min within 24 hours prior to randomization
  • Hemodynamic instability at time of screening
  • Body mass index > 40
  • Extra-cardiac illness that is expected to limit survival to less than 3 years
  • Participation or planned participation in another investigational intervention study within 60 days prior to randomization
  • Unable to give informed consent or potential for noncompliance with the study protocol due to psychiatric illness, organic brain disease, dementia, current alcohol abuse, mental retardation, language barrier, or geographical inaccessibility;
  • Pregnancy at time of screening or intention to become pregnant

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Modelli osservazionali: Coorte
  • Prospettive temporali: Prospettiva

Coorti e interventi

Gruppo / Coorte
Angiogram Review Group
All consecutive and consenting patients undergoing diagnostic cardiac catheterization in a 3 month period
Therapeutic Intervention Group
  • Cohort 2 Therapeutic Intervention Group - HCR Patients (including those from the angiogram review group) who undergo Hybrid coronary revascularization (HCR) with minimally invasive LIMA-LAD CABG, OR
  • Cohort 2 Therapeutic Intervention Group - PCI Patients (including those from the angiogram review group) who meet the proposed anatomic and clinical eligibility criteria and undergo multivessel Percutaneous Coronary Intervention with Drug Eluting Stents

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Major Adverse Cardiac and Cerebrovascular Event (MACCE)
Lasso di tempo: Month 12

For the purposes of this study MACCE is defined as a non-weighted composite score comprised of the following components:

  • Death
  • Stroke
  • Myocardial Infarction
  • Repeat Revascularization
Month 12

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Major Adverse Cardiac and Cerebrovascular Event (MACCE)
Lasso di tempo: Occurence of MACCE through the end of study up to two years

For the purposes of this study MACCE is defined as a non-weighted composite score comprised of the following components:

  • Death
  • Stroke
  • Myocardial infarction
  • Repeat revascularization
Occurence of MACCE through the end of study up to two years

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: John Puskas, MD, MSc, FACS, FACC, Emory University
  • Investigatore principale: Deborah Ascheim, MD, Icahn School of Medicine at Mount Sinai (Data Coordinating Center)
  • Investigatore principale: Joseph J DeRose, MD, FACS, Montefiore Medical Center
  • Investigatore principale: Michael Argenziano, MD, FACS, Columbia University
  • Investigatore principale: Mathew Williams, MD, Columbia University
  • Investigatore principale: John G. Byrne, MD, Vanderbilt University Medical Center

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio

1 maggio 2010

Completamento primario (Effettivo)

1 agosto 2012

Completamento dello studio (Effettivo)

1 agosto 2013

Date di iscrizione allo studio

Primo inviato

10 maggio 2010

Primo inviato che soddisfa i criteri di controllo qualità

11 maggio 2010

Primo Inserito (Stima)

12 maggio 2010

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Stima)

14 marzo 2014

Ultimo aggiornamento inviato che soddisfa i criteri QC

7 febbraio 2014

Ultimo verificato

1 febbraio 2014

Maggiori informazioni

Termini relativi a questo studio

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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