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

torstai 8. joulukuuta 2016 päivittänyt: 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.

Tutkimuksen yleiskatsaus

Yksityiskohtainen kuvaus

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.

Opintotyyppi

Havainnollistava

Ilmoittautuminen (Todellinen)

183

Yhteystiedot ja paikat

Tässä osiossa on tutkimuksen suorittajien yhteystiedot ja tiedot siitä, missä tämä tutkimus suoritetaan.

Opiskelupaikat

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

Osallistumiskriteerit

Tutkijat etsivät ihmisiä, jotka sopivat tiettyyn kuvaukseen, jota kutsutaan kelpoisuuskriteereiksi. Joitakin esimerkkejä näistä kriteereistä ovat henkilön yleinen terveydentila tai aiemmat hoidot.

Kelpoisuusvaatimukset

Opintokelpoiset iät

18 vuotta - 75 vuotta (Aikuinen, Vanhempi Aikuinen)

Hyväksyy terveitä vapaaehtoisia

Ei

Sukupuolet, jotka voivat opiskella

Kaikki

Näytteenottomenetelmä

Todennäköisyysnäyte

Tutkimusväestö

Patients with cardiovascular disease

Kuvaus

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

Opintosuunnitelma

Tässä osiossa on tietoja tutkimussuunnitelmasta, mukaan lukien kuinka tutkimus on suunniteltu ja mitä tutkimuksella mitataan.

Miten tutkimus on suunniteltu?

Suunnittelun yksityiskohdat

  • Havaintomallit: Kohortti
  • Aikanäkymät: Tulevaisuuden

Mitä tutkimuksessa mitataan?

Ensisijaiset tulostoimenpiteet

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

Toissijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Acute procedural success
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: At time of intervention, and at 6, 12, 24, 36 months
At time of intervention, and at 6, 12, 24, 36 months
Cardiac death
Aikaikkuna: At time of intervention, and at 6, 12,24, 36 months
At time of intervention, and at 6, 12,24, 36 months
Myocardial infarction
Aikaikkuna: 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)
Aikaikkuna: 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)
Aikaikkuna: 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)
Aikaikkuna: at 6, 12, 24, 36 months
TVR is ischemia driven.
at 6, 12, 24, 36 months
Ischemia driven target vessel failure (TVF)
Aikaikkuna: at 6, 12, 24, 36 month
at 6, 12, 24, 36 month
In-lesion % diameter stenosis
Aikaikkuna: Prior procedure
Prior procedure
In-scaffold % diameter stenosis
Aikaikkuna: At time of intervention and at angiographic FU if applicable
At time of intervention and at angiographic FU if applicable
Minimal lumen diameter (MLD)
Aikaikkuna: Prior and post procedure and at FU if applicable
Prior and post procedure and at FU if applicable
In-scaffold late lumen loss (LLL)
Aikaikkuna: At angiographic follow-up if applicable
At angiographic follow-up if applicable
Proximal and distal late lumen loss (LLL)
Aikaikkuna: At angiographic follow-up if applicable
At angiographic follow-up if applicable
In-lesion late lumen loss
Aikaikkuna: At angiographic follow-up if applicable
At angiographic follow-up if applicable
Response to nitroglycerin
Aikaikkuna: Before scaffold implantation, during angiographic follow-up if applicable
Before scaffold implantation, during angiographic follow-up if applicable
In-lesion angiographic binary restenosis (≥ 50%)
Aikaikkuna: At angiographic follow-up if applicable
At angiographic follow-up if applicable
Curvature (cm-1)
Aikaikkuna: 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 (°)
Aikaikkuna: 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
Aikaikkuna: 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)
Aikaikkuna: at 6, 12, 24, 36 month
at 6, 12, 24, 36 month

Yhteistyökumppanit ja tutkijat

Täältä löydät tähän tutkimukseen osallistuvat ihmiset ja organisaatiot.

Yhteistyökumppanit

Tutkijat

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

Julkaisuja ja hyödyllisiä linkkejä

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Yleiset julkaisut

Opintojen ennätyspäivät

Nämä päivämäärät seuraavat ClinicalTrials.gov-sivustolle lähetettyjen tutkimustietueiden ja yhteenvetojen edistymistä. National Library of Medicine (NLM) tarkistaa tutkimustiedot ja raportoidut tulokset varmistaakseen, että ne täyttävät tietyt laadunvalvontastandardit, ennen kuin ne julkaistaan ​​julkisella verkkosivustolla.

Opi tärkeimmät päivämäärät

Opiskelun aloitus

Sunnuntai 1. huhtikuuta 2012

Ensisijainen valmistuminen (Todellinen)

Perjantai 1. maaliskuuta 2013

Opintojen valmistuminen (Todellinen)

Keskiviikko 1. kesäkuuta 2016

Opintoihin ilmoittautumispäivät

Ensimmäinen lähetetty

Tiistai 17. huhtikuuta 2012

Ensimmäinen toimitettu, joka täytti QC-kriteerit

Perjantai 20. huhtikuuta 2012

Ensimmäinen Lähetetty (Arvio)

Tiistai 24. huhtikuuta 2012

Tutkimustietojen päivitykset

Viimeisin päivitys julkaistu (Arvio)

Perjantai 9. joulukuuta 2016

Viimeisin lähetetty päivitys, joka täytti QC-kriteerit

Torstai 8. joulukuuta 2016

Viimeksi vahvistettu

Torstai 1. joulukuuta 2016

Lisää tietoa

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