- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT00606333
Comparison of the Conor Sirolimus-eluting Coronary Stent to the Taxus Liberte Paclitaxel-eluting Coronary Stent in the Treatment of Coronary Artery Lesions (NEVO RES-I)
A Randomized, Multi-Center, Single-Blind Comparison of the Conor Cobalt Chromium Reservoir Based Stent With Sirolimus Elution Versus the TAXUS Liberte Paclitaxel-eluting Coronary Stent System in De Novo Native Coronary Artery Lesions
The purpose of this study is to evaluate the safety and effectiveness of the Conor Sirolimus-eluting Coronary Stent System in the treatment of coronary artery disease (a single atherosclerotic lesion) in native coronary arteries. The study will evaluate the outcomes of a new drug-eluting stent compared to an approved drug-eluting stent.
While Cordis made a business decision to no longer pursue NEVO™ development and commercialization, the patients will be followed up as per protocol. This includes performing all protocol required follow-up visits and the collection and reporting of all safety information.
Panoramica dello studio
Stato
Condizioni
Descrizione dettagliata
Restenosis remains a frequent cause of late failure following successful coronary angioplasty occurring in an estimated 20-40% of procedures performed. Coronary stents provide mechanical scaffolding that helps reduce restenosis by limiting the extent of elastic recoil and late vascular remodeling. Despite improvements over balloon angioplasty alone, restenosis following coronary stenting procedures has been cited to occur in 20-40% of cases and is primarily a result of neointimal hyperplasia. Thus, stents which are capable of delivering drugs to limit neointimal hyperplasia, in addition to providing mechanical support at the area of the lesion, have been developed to further limit the extent of restenosis following coronary stenting. There are several pharmacologic agents approved for use with drug-eluting stents.Two drugs have been widely studied in controlled clinical trials and real-world patient populations, sirolimus and paclitaxel.
This study will evaluate a new sirolimus-eluting cobalt chromium coronary stent system compared to an approved paclitaxel-eluting coronary stent system in the treatment of single de novo coronary lesions in native coronary arteries. Subjects meeting qualification will be randomized in a 1:1 fashion to treatment with the Conor sirolimus-eluting coronary stent or to treatment with an approved paclitaxel-eluting coronary stent. All subjects will undergo angiographic follow-up at six months and complete clinical follow-up for a period of five years.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
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Sao Paulo, Brasile, 04012-909
- Instituto Dante Pazzanese de Cardiologia
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Auckland
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Epsom, Auckland, Nuova Zelanda
- Mercy Angiography Unit
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- 18 years of age or older
- Eligible for percutaneous coronary intervention and coronary artery bypass graft surgery.
- Diagnosis of stable or unstable angina or silent ischemia
- Left ventricular ejection fraction >30%
- The subject requires treatment of a single de novo lesion in a native coronary artery.
- Lesion to be treated is less than or equal to 28 mm in length in a vessel that is 2.5-3.5mm diameter.
- The target lesion diameter stenosis is >50% and <100% by visual estimate.
- The target lesion is a minimum of 10 mm distance from any previously treated segment of the target vessel.
- The subject understands the study requirements, is willing to comply with all study procedures and has provided written informed consent.
Exclusion Criteria:
- The subject has undergone coronary revascularization to any vessel within 30 days.
- The subject has undergone target vessel revascularization within 6 months.
- Treatment of more than one qualifying lesion is required at the time of enrollment, or is planned within 30 days following enrollment.
- The subject has known sensitivity to sirolimus, paclitaxel, the polymeric matrices, stainless steel or cobalt chromium.
- There is planned treatment of the target lesion with any device other than the pre-dilatation balloon angioplasty catheter.
- The subject had a myocardial infarction within 72 hours, or presents with CK elevation > 2 times upper limit normal associated with elevated CK-MB.
- The subject is in cardiogenic shock.
- The subject had a cerebrovascular accident within the past 6 months.
- The subject has acute or chronic renal dysfunction (defined as creatinine >2.0 mg/dl).
- The subject has a contraindication to aspirin or clopidogrel.
- The subject has thrombocytopenia (platelet count < 100,000/mm3.
- The subject has had active gastrointestinal bleeding within the past 3 months.
- The subject has a known bleeding or hypercoagulable disorder.
- The subject has had prior anaphylactoid reaction to contrast agents or has contrast sensitivity that cannot be controlled with pre-medication.
- The subject is currently taking immunosuppressant therapy.
- The subject is currently, or has been treated wtih either Rapamune or paclitaxel within 12 months of the procedure.
- The subject is a female with a positive pregnancy test or is lactating.
- The subject has an active infection.
- The subject has co-morbidities that could interfere wtih completion of study procedures, or life expectancy less than 24 months.
- The subject is participating in another investigational drug or device trial that has not completed the primary endpoint or would interfere with the endpoints of this study.
Angiographic Exclusion Criteria
- Left main disease >50% diameter stenosis.
- The target lesion is ostial.
- The target lesion or target vessel are severely calcified.
- The target lesion involves a bifurcation with diseased branch vessel greater than or equal to 2.0 mm that would require intervention or protection.
- The target lesion has TIMI o or TIMI I flow.
- Angiographic evidence of thrombus.
- The target vessel has had prior stent placement.
- The patient has had prior coronary brachytherapy.
- There is angiographic restenosis of any previously treated segment of the target vessel, or atherosclerotic area wtih >50% diameter stenosis outside of the target lesion.
- The subject has undergone prior CABG.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Separare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
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Sperimentale: Investigational arm
Subjects randomized to treatment with the NEVO™ Sirolimus-eluting Coronary Stent System.
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Intervention will consist of percutaneous coronary intervention for treatment of a single coronary lesion using standard coronary intervention techniques.
Intervention in this arm will include treatment with the Conor Cobalt Chromium Sirolimus-eluting Coronary Stent System.
Subjects assigned to the IVUS sub-study population will undergo intravascular ultrasound evaluation immediately post-stenting.
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Comparatore attivo: Control Arm
Subjects randomized to treatment with the TAXUS Liberte Paclitaxel-eluting Coronary Stent System.
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Intervention will consist of percutaneous coronary intervention for treatment of a single coronary lesion using standard coronary intervention techniques.
Intervention in this arm will include treatment with the TAXUS Liberte Paclitaxel-eluting Coronary Stent System.
Subjects assigned to the IVUS sub-study population will undergo intravascular ultrasound evaluation immediately post-stenting.
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
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Angiographic endpoint of in-stent late lumen loss as measured by QCA.
Lasso di tempo: 6 months
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6 months
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Misure di risultato secondarie
Misura del risultato |
Lasso di tempo |
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Target Lesion Failure defined as cardiac death that cannot be clearly attributed to a non-cardiac event or non-target vessel, target vessel related myocardial infarction or clinically driven target lesion revascularization.
Lasso di tempo: hospital discharge, 30 days, 6 months and annually through five years.
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hospital discharge, 30 days, 6 months and annually through five years.
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Target Vessel Failure defined as any myocardial infarction or cardiac death that cannot be attributed to a non-target vessel or any target vessel revascularization.
Lasso di tempo: Hospital discharge, 30 days, 6 months and annually through five years
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Hospital discharge, 30 days, 6 months and annually through five years
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Major Adverse Cardiac Events defined as an adjudicated composite of death, emergent coronary artery bypass graft surgery, target lesion revascularization, or new myocardial infarction.
Lasso di tempo: Hospital discharge, 30 days, 6 months and annually through five years
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Hospital discharge, 30 days, 6 months and annually through five years
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Incidence of stent thrombosis
Lasso di tempo: Hospital discharge, 30 days, 6 months and annually through five years
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Hospital discharge, 30 days, 6 months and annually through five years
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Incidence of target lesion revascularization and target vessel revascularization.
Lasso di tempo: Hospital discharge, 30 days, 6 months and annually through five years
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Hospital discharge, 30 days, 6 months and annually through five years
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Device Success
Lasso di tempo: Procedural
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Procedural
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Lesion success
Lasso di tempo: Procedural
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Procedural
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Procedure Success
Lasso di tempo: Hospital Discharge
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Hospital Discharge
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Angiographic in-stent and in-segment binary restenosis.
Lasso di tempo: 6 months
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6 months
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In-stent minimum lumen diameter
Lasso di tempo: 6 months
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6 months
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Percent volume obstruction of the stent by intravascular ultrasound evaluation
Lasso di tempo: 6 months
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6 months
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Patient reported outcomes as measured by three standardized quality of life surveys.
Lasso di tempo: Baseline, 30 days, 6 months and 12 months
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Baseline, 30 days, 6 months and 12 months
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Collaboratori e investigatori
Sponsor
Collaboratori
Investigatori
- Investigatore principale: John Ormiston, MB ChM, Mercy Angiography Unit
- Investigatore principale: Alexandre Abizaid, MD. PhD, Instituto Dante Pazzanese de Cardiologia
Pubblicazioni e link utili
Pubblicazioni generali
- Ormiston JA, Abizaid A, Spertus J, Fajadet J, Mauri L, Schofer J, Verheye S, Dens J, Thuesen L, Dubois C, Hoffmann R, Wijns W, Fitzgerald PJ, Popma JJ, Macours N, Cebrian A, Stoll HP, Rogers C, Spaulding C; NEVO ResElution-I Investigators. Six-month results of the NEVO Res-Elution I (NEVO RES-I) trial: a randomized, multicenter comparison of the NEVO sirolimus-eluting coronary stent with the TAXUS Liberte paclitaxel-eluting stent in de novo native coronary artery lesions. Circ Cardiovasc Interv. 2010 Dec;3(6):556-64. doi: 10.1161/CIRCINTERVENTIONS.110.946426. Epub 2010 Nov 9. Erratum In: Circ Cardiovasc Interv. 2011 Feb 1;4(1):e4.
- Otake H, Honda Y, Courtney BK, Shimohama T, Ako J, Waseda K, Macours N, Rogers C, Popma JJ, Abizaid A, Ormiston JA, Spaulding C, Cohen SA, Fitzgerald PJ. Intravascular ultrasound results from the NEVO ResElution-I trial: a randomized, blinded comparison of sirolimus-eluting NEVO stents with paclitaxel-eluting TAXUS Liberte stents in de novo native coronary artery lesions. Circ Cardiovasc Interv. 2011 Apr 1;4(2):146-54. doi: 10.1161/CIRCINTERVENTIONS.110.957175. Epub 2011 Mar 8.
- Abizaid A, Ormiston JA, Fajadet J, Mauri L, Schofer J, Verheye S, Dens J, Thuesen L, Macours N, Qureshi AC, Spaulding C; NEVO ResElution-I Investigators. Two-year follow-up of the NEVO ResElution-I(NEVO RES-I) trial: a randomised, multicentre comparison of the NEVO sirolimus-eluting coronary stent with the TAXUS Liberte paclitaxel-eluting stent in de novo native coronary artery lesions. EuroIntervention. 2013 Oct;9(6):721-9. doi: 10.4244/EIJV9I6A116.
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Malattie cardiache
- Malattia cardiovascolare
- Malattie vascolari
- Arteriosclerosi
- Malattie arteriose occlusive
- Malattia coronarica
- Disfunsione dell'arteria coronaria
- Ischemia miocardica
- Aterosclerosi
- Effetti fisiologici delle droghe
- Meccanismi molecolari dell'azione farmacologica
- Agenti antinfettivi
- Agenti antineoplastici
- Agenti immunosoppressivi
- Fattori immunologici
- Modulatori della tubulina
- Agenti antimitotici
- Modulatori della mitosi
- Agenti antineoplastici, fitogenici
- Agenti antibatterici
- Antibiotici, Antineoplastici
- Agenti antimicotici
- Paclitaxel
- Paclitaxel legato all'albumina
- Sirolimo
Altri numeri di identificazione dello studio
- CP-06
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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