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ABSORB: Postmarketing Surveillance Registry to Monitor the Everolimus-eluting Bioresorbable Vascular Scaffold in Patients With Coronary Artery Disease (ASSURE)

8 december 2016 bijgewerkt door: Detlef Mathey, Medical Care Center Prof. Mathey, Prof. Schofer, Ltd.

ABSORB: Initial Clinical Experience With the Everolimus-eluting Bioresorbable Vascular Scaffold (BVS) System in the Treatment of de Novo Native Coronary Artery Lesions - a Surveillance Registry

The registry aims to evaluate the safety, performance and efficacy of the Everolimus-eluting bioresorbable vascular scaffold (BVS) system in patients with de novo native coronary artery lesions in all-day clinical practice.

Studie Overzicht

Gedetailleerde beschrijving

Bioresorbable scaffolds are transient implants. They act like drug-eluting metallic stents (DES) during the first 3 months by supporting the vessel wall thereby keeping the artery patent. Subsequently, resorption of the scaffold begins and its structure loosens. As a result of everolimus release, neointimal growth is inhibited similar to DES. Finally the implant is reabsorbed completely in about 2-3 years. BVS in terms of late stent thrombosis may be safer than DES. Transiently scaffolded vessels may regain their natural curvature and angulation as well as response to nitroglycerine and endothelial function.

Studietype

Observationeel

Inschrijving (Werkelijk)

183

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

      • Bernau, Duitsland, 16321
        • Herzzentrum Brandenburg in Bernau
      • Coburg, Duitsland, 96450
        • Klinikum Coburg GmbH
      • Essen, Duitsland, 45138
        • Elisabeth-Krankenhaus Essen GmbH
      • Hamburg, Duitsland, 22527
        • Medical Care Center Prof. Mathey, Prof. Schofer GmbH
      • Kiel, Duitsland, 24105
        • Universitatsklinikum Schleswig-Holstein
      • Ulm, Duitsland, 89081
        • Universitätsklinikum Ulm

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar tot 75 jaar (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Bemonsteringsmethode

Kanssteekproef

Studie Bevolking

Patients with cardiovascular disease

Beschrijving

The recommendation to implant BVS in an individual patient is purely based on clinical grounds. These are determined by the instructions for use (IFU) of the BVS and by the clinical experience accumulated so far from clinical studies.These studies suggest that the BVS should be implanted under certain conditions, which are determined by the patient and the coronary lesion treated:

Eligible:

Regarding to patient

  • Patient ≥ 18 and ≤ 75 years with a live expectancy of at least 5 years with ischemic heart disease (chronic, NSTEMI and unstable angina) due to one or more de novo native coronary artery lesions
  • Patients with evidence of myocardial ischemia

Regarding to lesion

  • Reference vessel diameter ≥ 2.0 mm and ≤ 3.8 mm, visually estimated and by online QCA
  • Percent diameter stenosis ≥ 50% and < 100%, visually estimated and by online QCA
  • TIMI ≥1
  • Previous interventions of target vessel lesions should have been done ≥ 6 months prior to index procedure and > 10 mm distal to the target lesion
  • Previous interventions of non-target vessel lesions should have been done ≥ 30 days prior to index procedure
  • In case of >1 target lesions, those should be from different epicardial vessels

Not eligible:

Regarding to patient

  • Patient in whom antiplatelet therapy and/or anticoagulant therapy is contraindicated
  • Patient with a known hypersensitivity or contraindication to aspirin, both heparin and bivalirudin, clopidogrel, ticlopidine, prasugrel and ticagrelor, everolimus, poly (L-lactide), poly (D,L-lactide), or platinum, or with contrast sensitivity, who cannot be adequately premedicated
  • Patient has a known diagnosis of acute myocardial infarction (STEMI) within 72 hours preceding the index procedure and CK and CK-MB have not returned within normal limits at the time of procedure
  • Patient is currently experiencing clinical symptoms consistent with STEMI
  • Patient has current unstable arrhythmias
  • Patient has a known left ventricular ejection fraction < 30%
  • Patient has received a heart transplant or any other organ transplant or is waiting for any organ transplant
  • Patient receiving or scheduled to receive chemotherapy for malignancy within 30 days prior to or after procedure
  • Patient is receiving immunosuppression therapy and has known immunosuppressive or autoimmune disease
  • Patient is receiving or scheduled to receive chronic anticoagulation therapy
  • Elective surgery is planned within the first 6 month after the procedure that will require discontinuing either aspirin or clopidogrel
  • Patient has a platelet count < 100 000 cells/mm3 or > 700 000 cells/mm3, a WBC of
  • < 3000 cells/mm3, or documented or suspected liver disease
  • Patient has known renal insufficiency
  • Patient has a history of bleeding diathesis or coagulopathy or will refuse blood transfusions
  • Patient has cerebrovascular accident or transient ischemic neurological attack within the past six month
  • Patient has had a significant GI or urinary bleed within the past six months
  • Patient has extensive peripheral vascular disease that precludes safe 6 French sheath insertion
  • Patient has other medical illness (e.g., cancer or congestive heart failure) or known history of substance abuse (alcohol, cocaine, heroin etc.) that may cause non.compliance with the clinical study plan, confound the data interpretation or is associated with a limited life expectancy (i.e., les than one year)
  • Women of childbearing potential who have not undergone surgical sterilization or are not post-menopausal

Regarding to lesion

  • Aorto-ostial location
  • Left main location
  • Located within 2 mm of the origin of LAD or LCX
  • Located within an arterial or saphenous vein graft or distal to a diseased (defined as vessel irregularity per angiogram and > 20% stenosed lesion by visual estimation) arterial or saphenous vein graft
  • Lesion involving a bifurcation with side branch vessel ≥ 2 mm in diameter, ostial lesion > 40% stenosed by visual estimation or side branch requiring predilation
  • Total occlusion (TIMI flow 0), prior to wire passing
  • Excessive tortuosity proximal to or within the lesion (extreme angulation (≥ 90°) proximal to or within the lesion)
  • Heavy calcification
  • Restenotic from previous intervention
  • Target vessel is containing thrombus

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Observatiemodellen: Cohort
  • Tijdsperspectieven: Prospectief

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
(This trial has no primary outcome, all outcomes are of equal weight), Major Adverse Cardiac Event (MACE)
Tijdsspanne: at 24 months
Composite of ischemia driven target lesion revascularisation (TLR), myocardial infarction and cardiac death
at 24 months

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Acute procedural success
Tijdsspanne: At the end of hospital stay (maximum of 7 days)
Achievement of final in-scaffold residual stenosis of < 50% and TIMI flow 3 of the target site. Successful delivery and deployment of at least one study scaffold at the intended target lesion and successful withdrawal of the delivery system for all target lesions without occurrence of cardiac death, target vessel MI or repeat TLR during hospital stay (maximum of 7 days). In dual target lesion setting both lesions must meet clinical procedure success criteria.
At the end of hospital stay (maximum of 7 days)
Acute device success
Tijdsspanne: At time of intervention
Successful delivery and deployment of the first scaffold at the intended target lesion (in overlapping setting both planned scaffolds) and successful withdrawal of delivery system. Attainment of < 50 % residual stenosis and TIMI flow 3 of the target site, using the BVS without the need for other non- study stents.
At time of intervention
Scaffold thrombosis
Tijdsspanne: At time of intervention, and at 6, 12, 24, 36 months
At time of intervention, and at 6, 12, 24, 36 months
Cardiac death
Tijdsspanne: At time of intervention, and at 6, 12,24, 36 months
At time of intervention, and at 6, 12,24, 36 months
Myocardial infarction
Tijdsspanne: At time of intervention, and at 6, 12, 24 36 months
At time of intervention, and at 6, 12, 24 36 months
Ischemia driven target lesion revascularisation (TLR)
Tijdsspanne: At time of intervention, and at 6, 12, 24, 36 months
Target lesion denominates scaffolded segment and 5 mm beyond.
At time of intervention, and at 6, 12, 24, 36 months
Major Adverse Cardiac Event (MACE)
Tijdsspanne: At time of intervention, participants will be followed for the duration of hospital stay (an expected average of 3 days), at 6, 12, 36 months
Composite of ischemia driven target lesion revascularisation (TLR), myocardial infarction and cardial death
At time of intervention, participants will be followed for the duration of hospital stay (an expected average of 3 days), at 6, 12, 36 months
Ischemia driven target vessel revascularisation (TVR)
Tijdsspanne: at 6, 12, 24, 36 months
TVR is ischemia driven.
at 6, 12, 24, 36 months
Ischemia driven target vessel failure (TVF)
Tijdsspanne: at 6, 12, 24, 36 month
at 6, 12, 24, 36 month
In-lesion % diameter stenosis
Tijdsspanne: Prior procedure
Prior procedure
In-scaffold % diameter stenosis
Tijdsspanne: At time of intervention and at angiographic FU if applicable
At time of intervention and at angiographic FU if applicable
Minimal lumen diameter (MLD)
Tijdsspanne: Prior and post procedure and at FU if applicable
Prior and post procedure and at FU if applicable
In-scaffold late lumen loss (LLL)
Tijdsspanne: At angiographic follow-up if applicable
At angiographic follow-up if applicable
Proximal and distal late lumen loss (LLL)
Tijdsspanne: At angiographic follow-up if applicable
At angiographic follow-up if applicable
In-lesion late lumen loss
Tijdsspanne: At angiographic follow-up if applicable
At angiographic follow-up if applicable
Response to nitroglycerin
Tijdsspanne: Before scaffold implantation, during angiographic follow-up if applicable
Before scaffold implantation, during angiographic follow-up if applicable
In-lesion angiographic binary restenosis (≥ 50%)
Tijdsspanne: At angiographic follow-up if applicable
At angiographic follow-up if applicable
Curvature (cm-1)
Tijdsspanne: Prior and post procedure and at angiographic follow-up if applicable
treated region
Prior and post procedure and at angiographic follow-up if applicable
Angulation (°)
Tijdsspanne: Prior and post procedure and at angiographic follow-up if applicable
Treated region
Prior and post procedure and at angiographic follow-up if applicable
Clinical success
Tijdsspanne: At time of intervention, and at 6, 12, 24, 36 months
Procedural success and freedom from TVF, TVR, CABG and scaffold thrombosis
At time of intervention, and at 6, 12, 24, 36 months
Coronary artery bypass grafting (CABG)
Tijdsspanne: at 6, 12, 24, 36 month
at 6, 12, 24, 36 month

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Hoofdonderzoeker: Detlef G Mathey, MD, Medical Care Center Prof. Mathey, Prof. Schofer GmbH

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Algemene publicaties

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start

1 april 2012

Primaire voltooiing (Werkelijk)

1 maart 2013

Studie voltooiing (Werkelijk)

1 juni 2016

Studieregistratiedata

Eerst ingediend

17 april 2012

Eerst ingediend dat voldeed aan de QC-criteria

20 april 2012

Eerst geplaatst (Schatting)

24 april 2012

Updates van studierecords

Laatste update geplaatst (Schatting)

9 december 2016

Laatste update ingediend die voldeed aan QC-criteria

8 december 2016

Laatst geverifieerd

1 december 2016

Meer informatie

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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