Study Comparing Onyx and TRUFILL in Brain Arteriovenous Malformations (AVMs)

NCT ID: NCT00857662

Last Updated: 2023-10-27

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 117 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2001-05-31
• Study Completion Date: 2007-12-31

Brief Summary

Test whether AVMs treated with Onyx is equivalent to treatment with n-BCA. Success is defined as an AVM size reduction greater than 50%

Detailed Description

Recent advances in the endovascular treatment of arteriovenous malformations (AVMs) have increased the number of patients with brain AVMs for whom embolization therapy may be appropriate. The permanency of obliterated nidi and occurrence of procedural complications are thought to be at least partially influenced by the characteristics of the material used, with liquid agents more likely to reach and occlude the AVM nidus compared to particulate embolic agents.

The only liquid embolic agent approved in the U.S. for the presurgical embolization of AVMs is TRUFILL®. TRUFILL n-butyl cyanoacrylate (n-BCA) is a liquid adhesive that polymerizes into a solid material upon contact with blood fluids or tissue, via an anionic mechanism. TRUFILL Ethiodized Oil is mixed into the n-BCA monomer as a radiopaque polymerizing retardant. TRUFILL Tantalum Powder may also be added for radiopacity. The TRUFILL n-BCA Liquid Embolic System received U.S. FDA premarket approval on September 25, 2000 (P990040) for use in the embolization of cerebral AVMs, when presurgical devascularization is desired.

Onyx™ is a non-adhesive liquid embolic agent comprised of ethylene vinyl alcohol (EVOH) copolymer dissolved in dimethyl sulfoxide (DMSO), and of micronized tantalum powder. Onyx precipitates into a solid on contact with blood fluids, due to rapid diffusion of the DMSO solvent. The Onyx Liquid Embolic System received the European "CE mark" in July 1999, and has been available outside of the U.S. since September 1999 for use in the embolization of AVMs.

The purpose of this randomized-controlled study is to obtain prospective clinical data on the performance of Onyx (investigational device) and TRUFILL (control device) in the presurgical embolization of brain AVMs. Device safety will be assessed by comparing overall and device-related morbidity and mortality. The primary efficacy endpoint is the angiographic reduction in AVM size (volume) achieved. The objective is to demonstrate that Onyx is no worse than TRUFILL within a specified clinical tolerance. Study results will be used to support a premarket approval application for Onyx in the presurgical embolization of brain AVMs.

Conditions

Brain Arteriovenous Malformations

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Onyx

Group Type: EXPERIMENTAL

Onyx

Intervention Type: DEVICE

Embolization

TRUFILL

Group Type: ACTIVE_COMPARATOR

TRUFILL

Intervention Type: DEVICE

Embolization

Interventions

Onyx

Embolization

Intervention Type: DEVICE

TRUFILL

Embolization

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• The patient or patient's guardian understands and will sign the informed consent for the procedure
• The patient has a confirmed diagnosis of a brain AVM in the cerebral cortex, cerebellum or dura mater as visualized by angiography or cross sectional imaging.
• The brain AVM has a Spetzler-Martin grade of I, II, III, or IV. If the brain AVM has a Spetzler-Martin grade of I or II, the anticipated benefit of embolization for surgical resection is greater than the risk of the embolization procedure (e.g., patient stability).
• The patient is a candidate for surgical resection of the AVM post embolization.
• The patient is clinically and neurologically stable, for a minimum of 24 hours prior to embolization.
• The patient agrees to have, and is capable of completing, all study-related exams and procedures.
• Patient of any age.

Exclusion Criteria

• The patient is pregnant.
• The patient has a brain AVM with high flow arteriovenous fistulae that the investigator has determined to be unsuitable for embolization.
• The brain AVM has a Spetzler-Martin grade of V.
• The patient is participating in another research study involving another investigational device, procedure or drug.
• The brain AVM has been previously treated with another embolization agent

• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Micro Therapeutics Inc.

INDUSTRY

Sponsor Role: collaborator

Medtronic Neurovascular Clinical Affairs

INDUSTRY

Sponsor Role: lead

Responsible Party

Microtherapeutics, Inc dba ev3, Inc

Principal Investigators

Gary Duckwiler, MD

Role: PRINCIPAL_INVESTIGATOR

University of California, Los Angeles

Locations

UCLA

Los Angeles, California, United States

Countries

United States

Other Identifiers

G000296

Identifier Type: -

Identifier Source: org_study_id