Italian Absorb Registry
NCT02298413 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1520
Last updated 2016-02-04
Summary
The investigators aim at evaluating the long-term (5-year) clinical outcome following Absorb BVS implantation in a real world, all-comers population of consecutive patients, as treated according to the indications, techniques and protocols used in the participating institutions.
Conditions
Interventions
- DEVICE
-
PCI with Absorb scaffold
Implantation of biovascular scaffold during PCI
Sponsors & Collaborators
-
Fatebenefratelli and Ophthalmic Hospital
collaborator OTHER -
Bolognini Hospital
collaborator UNKNOWN -
Ospedale Regionale di Aosta
collaborator UNKNOWN -
Ospedali Riuniti di Ancona
collaborator UNKNOWN -
S. Giacomo Hospital
collaborator OTHER -
Azienda U.L.S.S n.9 Ospedale di Treviso Ca Foncello
collaborator UNKNOWN -
Ospedale San Bortolo di Vicenza
collaborator OTHER -
Azienda Ospedaliera Brotzu
collaborator OTHER -
San Giuseppe Moscati Hospital
collaborator OTHER -
Azienda Sanitaria Locale USL 13 Ospedale Mazzoni di Ascoli Piceno
collaborator UNKNOWN -
S. Andrea Hospital
collaborator OTHER -
Ospedale Monaldi di Napoli
collaborator UNKNOWN -
Azienda Ospedaliera di Padova
collaborator OTHER -
Ospedale della Misericordia di Grosseto
collaborator UNKNOWN -
Ospedale Santa Corona di Pietra Ligure
collaborator UNKNOWN -
Istituto Di Ricerche Farmacologiche Mario Negri
collaborator OTHER -
Ospedale Santa Croce-Carle Cuneo
lead OTHER
Principal Investigators
-
Alfonso Ielasi, MD · AO Seriate
-
Bernardo Cortese, MD · AO Fatebenefratelli
-
Donatella Corrado, PhD · Istituto Di Ricerche Farmacologiche Mario Negri
Eligibility
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-05-31
- Primary Completion
- 2016-11-30
- Completion
- 2021-05-31
Countries
- Italy
Study Locations
More Related Trials
-
SUPERa Stenting After SUBintimal Crossing of TASC C-D Femoro-popliteal Lesions in CLI Patients
NCT03452293 ·Status: COMPLETED
-
Single Long vs Two Short Overlapping Bioabsorbable Polymer DES
NCT01718106 ·Status: UNKNOWN ·Phase: NA
-
Italian Diffuse/Multivessel Disease ABSORB Prospective Registry: IT-Disappears
NCT02004730 ·Status: UNKNOWN ·Phase: PHASE4
-
To Evaluate the Performance and Safety of RisoR Crest Everolimus Eluting Coronary Stent System
NCT07098195 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Multicenter Postmarket Surveillance Registry Evaluating Performance and Long Term Safety of the Presillion Stent
NCT00968019 ·Status: COMPLETED
-
Bioresorbable Sirolimus-eluting scaffold in de Novo Coronary Artery Lesions
NCT07022587 ·Status: RECRUITING ·Phase: NA
-
Italian Multi-center Registry of Self-apposing Coronary Stent in Patients With STEMI
NCT02979236 ·Status: UNKNOWN
-
Intra-patient Study With Polymer Free Drug Eluting Stent Versus Abluminal Biodegradable Polymer Drug Eluting Stent With Early OCT (Optical Coherence Tomography) Follow up
NCT02785237 ·Status: COMPLETED ·Phase: NA
-
ABSORB Bioresorbable Scaffold vs. Xience Metallic Stent for Prevention of Restenosis in Patients at High Risk of Restenosis
NCT02486068 ·Status: UNKNOWN ·Phase: NA
-
MAGnesIum Alloy Scaffold for Coronary Artery Disease (MAGIC)
NCT04098042 ·Status: UNKNOWN
-
Trial of MiStent Compared to Xience in Japan
NCT02972671 ·Status: UNKNOWN ·Phase: NA
-
Self-apposing Stentys Stents Registry
NCT02784405 ·Status: UNKNOWN
-
Strut Coverage With SYNERGY Stents and Bioresorbable Vascular Scaffold in Acute Myocardial Infarction
NCT02890589 ·Status: COMPLETED ·Phase: NA
-
Costs, Effectiveness, QALYs, and Efficiency of Bioabsorbable Devices in Daily Clinical Practice
NCT02854007 ·Status: UNKNOWN
-
Optical Coherence Tomography in Long Lesions
NCT01133925 ·Status: UNKNOWN ·Phase: PHASE4
-
Bioabsorbable Versus Durable Polymer Drug Eluting Stent (DES): a Meta-analysis
NCT01466634 ·Status: COMPLETED
-
Stenting With or Without Coating Compared With Angioplasty in Non-benestent Disease
NCT00192881 ·Status: UNKNOWN ·Phase: NA
-
DISsection RE-entry Evaluation With Absorb Bioresorbable Vascular Scaffolds in CTO.
NCT02936011 ·Status: UNKNOWN ·Phase: NA
-
The Effects of Bindarit in Preventing Stent Restenosis
NCT01269242 ·Status: COMPLETED ·Phase: PHASE2
-
Ultrathin DES in Complex PCI Scenarios: the ULTRA a Multicenter Study
NCT05205148 ·Status: UNKNOWN
-
Safety and Efficacy of the Combo Bio-engineered Sirolimus-eluting Stent Versus the Nano Polymer-free Sirolimus-eluting Stent in the Treatment of Patients With de Novo Stenotic Lesions
NCT02542007 ·Status: COMPLETED ·Phase: NA
-
Everolimus-Eluting Bioresorbable Scaffolds Versus Everolimus-Eluting Metallic Stents for Diffuse Long Coronary Artery Disease
NCT02831205 ·Status: TERMINATED ·Phase: PHASE4
-
Everolimus Stent in Patients With Coronary Artery Disease (CAD)
NCT01182649 ·Status: COMPLETED ·Phase: PHASE3
-
International Randomized Comparison Between DES Limus Carbostent and Taxus DES in the Treatment of De-novo Coronary Lesions
NCT01373502 ·Status: COMPLETED ·Phase: NA
-
COMBO-Stent in Patients on Chronic Anticoagulant Therapy (COSTA) COSTA-Bleed and COSTA-Outcome Trials
NCT02723981 ·Status: WITHDRAWN ·Phase: PHASE4