ABSORB EXTEND Clinical Investigation

Abbott

Status

Completed

Conditions

Coronary Artery Disease

Myocardial Ischemia

Coronary Restenosis

Coronary Artery Stenosis

Coronary Disease

Cardiovascular Disease

Treatments

Device: ABSORB BVS

Study type

Interventional

Funder types

Industry

Identifiers

REFCTRI000460, 03-05-2010 (Registry Identifier)

09-386

ACTRN12610000131055 (Registry Identifier)

Details and patient eligibility

About

The ABSORB EXTEND trial is to continue the assessment of the safety and performance of the ABSORB Bioresorbable Vascular Scaffold (BVS) System

ABSORB BVS is currently in development at Abbott Vascular.

Enrollment

812 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Up to two de novo lesions can be treated, each located in a separate native epicardial vessel.
Target lesion(s) must be located in a native coronary artery where target vessel(s) diameter is ≥ 2.0 mm and ≤ 3.3 mm and target lesion length is ≤ 28 mm, both assessed by on-line Quantitative Coronary Analysis (QCA).
Target lesion(s) must be in a major artery or branch with a visually estimated stenosis of ≥ 50% and < 100% with a TIMI flow of ≥ 1.
If two treatable lesions meet the inclusion criteria they must be in separate major epicardial vessels (LAD with septal and diagonal branches, left circumflex artery (LCX) with obtuse marginal and/or ramus intermedius branches and right coronary artery (RCA) and any of its branches).
Percutaneous interventions for lesions in a non-target vessel are allowed if done ≥ 30 days prior to or if planned to be done 6 months after the index procedure.
Percutaneous intervention for lesions in the target vessel are allowed if done > 6 months prior to or if planned to be done 6 months after the index procedure.

Exclusion criteria

Lesion(s) 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(s) involving a bifurcation with side branch vessel ≥ 2 mm in diameter and/or ostial lesion > 40% stenosed by visual estimation or side branch requiring predilatation.
Total occlusion (TIMI flow 0), prior to wire passing.
Target vessel(s) contains visible thrombus.
Another clinically significant lesion is located in the same epicardial vessel (including side branch) as the target lesion(s).
Subject has received brachytherapy in any epicardial vessel (including side branches).