- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT01394848
Safety and Efficacy Study of Endothelial Progenitor Cell Capture Stent With 1 Months Dual Antiplatelet Therapy (INNOVATION)
EndothelIal progeNitor Cell Capture steNt With 1-mOnth Dual Antiplatelet Therapy Versus eVerolimus-eluting Stent With stAndard 12-month Dual anTIplatelet Therapy in Elderly (≥ 70 Year) With Stable corONary Artery Disease - INNOVATION Trial
Thanks to rapid reendothelialization derived from the pro-healing property of the EPC capture stent, 1-month dual antiplatelet therapy (DAPT) is recommended after EPC capture stent implantation. Shorter maintenance of dual antiplatelet therapy might minimize the risk for stent thrombosis in cases of discontinuation of antiplatelet regimen and prevent wasteful medications and bleeding complications related with dual antiplatelet therapy. Thus, the EPC capture stent might be valuable for the elderly because they are vulnerable to premature discontinuation of DAPT.
On the other hand, statin upstream therapy has gained popularity because it seems to reduce periprocedural myocardial injury especially in ACS through its pleiotrophic effect like plaque stabilization. However, the benefit of pretreatment of statin in patients with stable angina remains controversial. It is reported that statin administration could increase EPC level by accelerated differentiation towards the endothelial progenitor lineage.
We hypothesize that the EPC capture stent with 1-month dual antiplatelet therapy is non-inferior to DES in the elderly subjects with stable coronary artery disease. To test this hypothesis, we will perform a multi-center, randomized, prospective trial aimed at demonstrating the efficacy and safety of the EPC capture stent with 1-month DATP versus EES with standard 12-month DAPT in elderly patients with stable coronary occlusive disease in real world practice.
Panoramica dello studio
Stato
Condizioni
Descrizione dettagliata
Drug-eluting stents (DES) have improved angiographic and clinical outcomes in patients with the complex coronary lesions and high risks by markedly reducing the neointimal hyperplasia following stent implantation in comparison to bare-metal stents (BMS). Although the concerns about long-term safety and the occurrence of stent thrombosis following DES implantation had been raised, the recent DES-registry studies have reported that DES did not increase the risk of death or stent thrombosis during follow-up, as compared with BMS. However, currently, the fatal events related with stent thrombosis still occur and are the major limitation of the use of DES. Especially, late or very late thrombosis after DES implantation is an uncommon but life-threatening fatal complication presented with sudden death or myocardial infarction (MI).
The most powerful predictor for stent thrombosis is the discontinuation of clopidogrel. Then, under these circumstances, the prolonged dual antiplatelet therapy is now recommended, irrespective of each precise consideration according to the types of DES, lesion complexity, or clinical characteristics. Although the prolonged antiplatelet therapy can prevent stent thrombosis, it might cause other problems such as combined bleeding complications, high cost due to prolonged use, and unnecessary maintenance of medication. The stratified strategies regarding antiplatelet therapy according to the lesion complexity or high risks such as diabetes or acute coronary syndrome, which were regarded as the most prominent predictors for stent thrombosis, should be required. Another difficult problem of DES in real world practice is how we can manage the cases in which clopidogrel should be discontinued due to unexpected minor and major operations or invasive procedures. Because there have been no available substitutes as a bridging therapy of clopidogrel until operation, many advisory groups recommend to hold on off elective non-cardiac surgery 12 months after DES implantation. If not, BMS implantation is strongly recommended for patients with high risk of bleeding or scheduled unavoidable surgery within the next 12 months. Especially in the elderly, premature discontinuation of DAPT within 12 months after PCI may occur due to combined co-morbid disease requiring surgical intervention, decreased drug compliance, or occurrence of gastrointestinal bleeding.
Recently, many attempts to elucidate the mechanism of stent thrombosis have been performed. Finn AV et al. have reported from the human autopsies of DES that the most powerful histological predictor of stent thrombosis was endothelial coverage and suggested stent strut coverage as a marker of endothelialization. After then, the more concerns have been focused on the healthy healing after DES implantation, in spite of relatively higher late lumen loss. As a result, when antiplatelet therapy should be discontinued, DES with a healthy healing might be more preferred, instead of efficient DES with a lower late lumen loss.
In the view of these points, in spite of actual higher late lumen loss, Endothelial Progenitor Cell (EPC) Capture Stent (GENOUS™ Bio-engineered R stent™, OrbusNeich) could be more beneficial and safer than DES because of its low risk for stent thrombosis due to more rapid endothelialization and its resulting short-term use of dual antiplatelet. EPC capture stent has antibodies immobilized on the stent surface to capture circulating endothelial progenitor cells leading to accelerated natural healing. Theoretically, the EPC capture stent has two benefits. It establish functional endothelium, therefore no longer term anti-platelet therapy is required. Second, EPC capture stent may minimizes restenosis, because it establishes healthy endothelium which expresses vasoactive compounds, such as nitric oxide, which modulates neo-intimal hyperplasia and thus restenosis.
Thanks to rapid reendothelialization derived from the pro-healing property of the EPC capture stent, 1-month dual antiplatelet therapy (DAPT) is recommended after EPC capture stent implantation. Shorter maintenance of dual antiplatelet therapy might minimize the risk for stent thrombosis in cases of discontinuation of antiplatelet regimen and prevent wasteful medications and bleeding complications related with dual antiplatelet therapy. Thus, the EPC capture stent might be valuable for the elderly because they are vulnerable to premature discontinuation of DAPT.
On the other hand, statin upstream therapy has gained popularity because it seems to reduce periprocedural myocardial injury especially in ACS through its pleiotrophic effect like plaque stabilization. However, the benefit of pretreatment of statin in patients with stable angina remains controversial. It is reported that statin administration could increase EPC level by accelerated differentiation towards the endothelial progenitor lineage.
We hypothesize that the EPC capture stent with 1-month dual antiplatelet therapy is non-inferior to DES in the elderly subjects with stable coronary artery disease. To test this hypothesis, we will perform a multi-center, randomized, prospective trial aimed at demonstrating the efficacy and safety of the EPC capture stent with 1-month DATP versus EES with standard 12-month DAPT in elderly patients with stable coronary occlusive disease in real world practice.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Fase 4
Contatti e Sedi
Luoghi di studio
-
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Gangwon-do
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Wonju, Gangwon-do, Corea, Repubblica di, 220-701
- Yonsei University Wonju College of Medicine
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Age ≥70 years patients with coronary artery disease (≤stable angina CCS III, Unstable angina IIb
- patients with signed informed consent
- significant coronary artery stenosis (>50%) considered for coronary stenting
- Reference vessel diameter of 2.5 to 4.0 mm
Exclusion Criteria:
- The patient has a known hypersensitivity or contraindication to any of the following medications: Heparin, Aspirin, Clopidogrel, Everolimus, Contrast media (Patients with documented sensitivity to contrast media which can be effectively premedicated with steroids and diphenhydramine [e.g. rash] may be enrolled. Those with true anaphylaxis to prior contrast media, however, should not be enrolled.)
- Systemic (intravenous) Everolimus use within 12 months
- The patients who are receiving anticoagulants or anti-platelet medications besides aspirin & clopidogrel
- History of bleeding diathesis or known coagulopathy (including heparin-induced thrombocytopenia), or refuses blood transfusions
- Baseline hemogram with Hb<10g/dL or PLT count <100,000/μL
- Severe Hepatic dysfunction (≥ 3 times normal reference values)
- Significant renal dysfunction (Serum creatinine ≥ 2.0 mg/dl)
- Gastrointestinal or genitourinary bleeding within the prior 3 months, or major surgery within 2 months
- Patients with LV systolic dysfunction (LVEF<40%) or in cardiogenic shock
- Non-cardiac co-morbid conditions are present with life expectancy <1 year or that may result in protocol non-compliance (per site investigator's medical judgment)
- Patients who are actively participating in another drug or device investigational study, which have not completed the primary endpoint follow-up period
- An elective surgical procedure is planned that would necessitate interruption of DAPT during the first 12 months post enrollment
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione fattoriale
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Comparatore attivo: Genous stent group
Genous stent (Endothelial progenitor cell capture stent) insertion in elderly patients with stable coronary artery disease
|
75mg PO clopidogrel per day for 1 months
Altri nomi:
|
|
Comparatore attivo: Xience stent group
Xience Prime V stent (everolimus eluting stent) insertion in elderly patients with stable coronary artery disease
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75mg PO clopidogrel per day for over 12 months
Altri nomi:
|
|
Comparatore attivo: Atorvastatin 20mg group
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Atorvastatin 20mg loading before index percutaneous coronary intervention
Altri nomi:
|
|
Comparatore attivo: Atorvastatin 80mg group
|
Atorvastatin 80mg loading before index percutaneous coronary intervention
Altri nomi:
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Major adverse cardiovascular events
Lasso di tempo: 12 months
|
The incidence of the composite of cardiovascular death, non-fatal myocardial infarction (MI), target lesion revascularization (TLR), or stent thrombosis following randomly assigned coronary stent implantation
|
12 months
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Each component of the primary composite endpoint at 12 months
Lasso di tempo: 12 months
|
12 months
|
|
|
In-stent late loss and angiographic pattern of restenosis at 13 months
Lasso di tempo: 13 months
|
13 months
|
|
|
In-sent and in-segment % diameter stenosis (%DS) at 13 months
Lasso di tempo: 13 months
|
13 months
|
|
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Overall incidence of deferring or declining the request to discontinue dual antiplatelet between 1-12 months due to major and minor operations or invasive procedures
Lasso di tempo: 12 months
|
12 months
|
|
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Cost-reducing effect according the duration of duration of anti-platelet therapy
Lasso di tempo: 12 months
|
12 months
|
|
|
Periprocedural myocardial infarction
Lasso di tempo: 12 months
|
12 months
|
|
|
Bleeding defined by Bleeding Academic Research Consortium (BARC)
Lasso di tempo: 12 months
|
Bleeding Academic Research Consortium Definition for Bleeding Type 0 to Type 5
|
12 months
|
Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: Seung-Hwan Lee, MD, PhD, Yonsi university Wonju college of medicine, Wonju christian hospital
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
- Ischemia miocardica
- Malattie cardiache
- Malattia cardiovascolare
- Malattie vascolari
- Dolore
- Manifestazioni neurologiche
- Dolore al petto
- Angina pectoris
- Angina, Stabile
- Effetti fisiologici delle droghe
- Agenti neurotrasmettitori
- Meccanismi molecolari dell'azione farmacologica
- Inibitori enzimatici
- Inibitori dell'aggregazione piastrinica
- Antagonisti del recettore purinergico P2Y
- Antagonisti del recettore purinergico P2
- Antagonisti purinergici
- Agenti purinergici
- Antimetaboliti
- Agenti antineoplastici
- Agenti immunosoppressivi
- Fattori immunologici
- Agenti anticolesteremici
- Agenti ipolipidemizzanti
- Agenti regolatori dei lipidi
- Inibitori dell'idrossimetilglutaril-CoA reduttasi
- Atorvastatina
- Clopidogrel
- Everolimo
Altri numeri di identificazione dello studio
- INNOVATION_v5.0
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 .