NeoCast for Subdural Hematoma
(RADIANT Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new treatment called the NeoCast Embolic System, a medical device, to determine its safety and effectiveness for people with subacute or chronic subdural hematoma (a type of brain bleed), in conjunction with surgery. Researchers compare it to an already approved treatment to identify the best option for patients. Individuals who have experienced symptoms like headaches, speech difficulties, or seizures due to a subdural hematoma in the last 30 days might be suitable for this study. Participants must plan to undergo a specific procedure called middle meningeal artery embolization soon after their surgery. As an unphased trial, this study offers patients the chance to contribute to groundbreaking research that could enhance treatment options for subdural hematoma.
Do I have to stop taking my current medications for the NeoCast trial?
The trial does not specify if you need to stop taking your current medications, but if you are on anticoagulants (blood thinners), you must be able to stop them for at least 7 days after surgery.
What prior data suggests that the NeoCast Embolic System is safe for treating subdural hematoma?
Research has shown that the NeoCast Embolic System, used to treat subdural hematomas, is generally safe for patients. In previous studies, over 80% of patients who received NeoCast treatment recovered well without needing additional surgery. Additionally, no serious side effects, such as major strokes or death related to brain issues, were reported within 30 days after the procedure. This suggests that the treatment is well-tolerated. Although some risk accompanies any medical procedure, the evidence so far indicates that NeoCast is a safe option for many people.12345
Why are researchers excited about this trial's treatment?
Researchers are excited about the NeoCast Embolic System for treating subdural hematomas because it offers a novel approach compared to the current standard of care. Traditional treatments often involve surgical intervention alone, but NeoCast adds an embolic system that works alongside surgery to target the middle meningeal artery (MMA). This adjunctive method could potentially enhance surgical outcomes by reducing blood flow to the hematoma, thereby minimizing the risk of recurrence and promoting faster recovery. Additionally, the NeoCast system is designed to be more precise, which may lead to fewer complications and a more targeted treatment approach.
What evidence suggests that the NeoCast Embolic System is effective for subdural hematoma?
Research has shown that the NeoCast Embolic System could be a promising treatment for subdural hematomas, a type of brain bleed. In one study, 87% of patients experienced successful treatment without needing additional surgery. Another study found that all targeted blood vessels were successfully blocked without affecting other areas. The NeoCast material is designed to penetrate deeply into blood vessels and does not adhere to other tissues, ensuring it remains where needed. In this trial, participants will be randomized to receive either the NeoCast Embolic System or an FDA-approved commercial liquid embolic as an active comparator. These findings suggest that NeoCast could effectively help manage subdural hematomas.12678
Who Is on the Research Team?
Charles Matouk, MD
Principal Investigator
Yale Neurosciences Institute
Michael Levitt, MD
Principal Investigator
University of Washington Medicine - Harborview Medical Center
Are You a Good Fit for This Trial?
This trial is for adults aged 18–90 with a confirmed subacute or chronic subdural hematoma at least 10 mm thick, who have symptoms like headache, memory problems, speech issues, walking difficulties, weakness, or seizures. Participants must be scheduled for MMA embolization within a week of surgery and able to give consent.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants undergo embolization of the middle meningeal artery using either the NeoCast Embolic System or an FDA-approved commercial embolic adjunctive to surgery
Follow-up
Participants are monitored for safety and effectiveness, with primary effectiveness measured at 90 days and safety outcomes assessed through 180 days
What Are the Treatments Tested in This Trial?
Interventions
- NeoCast Embolic System
Trial Overview
The study tests the safety and effectiveness of using the NeoCast Embolic System (a device that blocks blood flow) in the middle meningeal artery to help treat subacute or chronic subdural hematomas after surgical removal. It compares this new system to an FDA-approved liquid embolic agent.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Active Control
Participants randomized to the NeoCast arm will have their MMA embolized with NeoCast adjunctive to surgery
Participants randomized to the active comparator control arm will have their MMA embolized with Onyx LES, an FDA-approved commercial liquid embolic adjunctive to surgery
Find a Clinic Near You
Who Is Running the Clinical Trial?
Arsenal Medical, Inc.
Lead Sponsor
Citations
MMA Embolization With NeoCast for Subacute and ...
The Primary Effectiveness Endpoint will be measured at the 90-day timepoint post-treatment. Participants will be followed through 180 days.
Arsenal's NeoCast Liquid Embolic Studied in EMBO-02 Trial
Arsenal Medical reported the following highlights from the data: 87% of patients underwent embolization without adjunctive surgery; 100% target ...
Imaging and Clinical Outcomes Six Months After Middle ... - PMC
Comparable procedural and radiological outcomes in both groups suggest embolization alone may suffice in select patients, offering a less ...
4.
ctv.veeva.com
ctv.veeva.com/study/mma-embolization-with-neocast-for-subacute-and-chronic-subdural-hematomaMMA Embolization With NeoCast for Subacute and Chronic ...
The purpose of this study is to evaluate the safety and efficacy of embolization of the middle meningeal artery (MMA) using the NeoCast ...
5.
neurosurgery.uw.edu
neurosurgery.uw.edu/research/grants-and-funding/pivotal-study-treatment-chronic-subdural-hematoma-middle-meningealPivotal Study of the Treatment of Chronic Subdural Hematoma ...
The primary objective of this pivotal study is the evaluation of the safety and effectiveness of MMA embolization with the Arsenal Medical ...
O-020 The EMBO-02 trial: middle meningeal artery ...
We report the results of EMBO-02, the first-in-human trial of NeoCast for Middle Meningeal Artery (MMA) embolization in patients with chronic subdural hematoma ...
EMBO-02 study
The enrollment of 25 participants is supported by evidence of the safety of NeoCast for use in the embolisation of chronic subdural hematomas based on ...
8.
medtechinnovator.org
medtechinnovator.org/nembo-02-study-indicates-rapid-csdh-resorption-and-pain-free-treatments-with-neocast-liquid-embolic-agent-featuring-arsenal-medical/NEMBO-02 study indicates rapid cSDH resorption and pain ...
Highlights from the study's results to date include 87% of patients undergoing embolisation without adjunctive surgery; 100% target vessel ...
Unbiased Results
We believe in providing patients with all the options.
Your Data Stays Your Data
We only share your information with the clinical trials you're trying to access.
Verified Trials Only
All of our trials are run by licensed doctors, researchers, and healthcare companies.