Enspire DBS Therapy Expands Stroke Treatment Clinical Trials
Enspire DBS Therapy Launches New Clinical Trial for Stroke Recovery
The recent milestone achieved by Enspire DBS Therapy, Inc. is a promising indication of progress in stroke recovery treatments. The company has successfully implanted the first patient at Brown University Health, marking a significant expansion of the RESTORE study to multiple clinical sites. This pivotal Phase 2/3 multicenter trial explores the combination of deep brain stimulation (DBS) and rehabilitation therapy (DBS + Rehab) in patients with chronic arm weakness following a stroke.
Understanding the RESTORE Initiative
RESTORE aims to generate essential data to support the long-term safety and efficacy of DBS combined with rehabilitation, ultimately seeking marketing approval for this innovative therapy. The trial is poised to include up to forty patients across nine clinical trial centers, building on the encouraging results from the earlier EDEN study. The EDEN trial showed that patients who underwent DBS + Rehab experienced significant improvements in both motor function and overall recovery.
Patient Impact and Potential
According to Dr. Wael Asaad, MD, PhD, Director of the Functional Neurosurgery & Epilepsy Program at Brown University Health, there is an urgent need for effective treatment alternatives for patients experiencing residual disabilities after a stroke. Many of these individuals face challenges that prevent a full return to their daily activities, highlighting the importance of new therapies like DBS + Rehab. Dr. Asaad expressed optimism that this emerging treatment could provide renewed hope for these patients.
Sites Participating in the RESTORE Trial
Currently, the RESTORE trial is active at several prestigious clinical hospitals, including Brown University Health, Cleveland Clinic, Massachusetts General Hospital, Mayo Clinic, and Medical University of South Carolina. Each of these facilities is working to recruit participants who meet the specific criteria for enrollment in this groundbreaking study.
Details of the Trial Structure
Each participant in RESTORE will receive a commercially available DBS system and participate in a five-month outpatient rehabilitation program. The study’s design is robust, as patients will be divided into two groups: an active-control group receiving traditional rehabilitation and a treatment group receiving the combined DBS + Rehab approach. After the initial five-month period, participants in the control group will have the opportunity to switch to the DBS treatment, further enriching the study’s data generation.
The Importance of Continued Research
Stroke remains one of the top causes of long-term disability in the United States, affecting approximately 800,000 individuals each year. While many patients survive the immediate aftermath of a stroke, the fallout can include substantial neurological challenges that diminish quality of life. The RESTORE trial represents a key effort in addressing these persistent disabilities, with the goal of contributing valuable information that could lead to effective solutions.
Conclusion on Stroke Rehabilitation Efforts
Incorporating innovative treatments like DBS for stroke recovery is vital for advancing the understanding and management of neural rehabilitation. With the support of clinical sites and dedicated healthcare professionals, the RESTORE trial aims to provide insight into new therapeutic approaches that can lead to improved outcomes for stroke survivors.
Frequently Asked Questions
What is the RESTORE trial about?
The RESTORE trial is a Phase 2/3 clinical study exploring the safety and effectiveness of deep brain stimulation combined with rehabilitation for treating arm weakness in stroke patients.
Who is eligible to participate in the trial?
Eligible participants are individuals who have chronic upper extremity impairment due to a stroke and meet specific inclusion criteria set by the trial.
Where is the RESTORE trial being conducted?
The trial is currently being conducted at clinical sites including Brown University Health, Cleveland Clinic, Massachusetts General Hospital, and Mayo Clinic, among others.
What is the goal of the RESTORE study?
The primary goal of RESTORE is to gather data to support the long-term safety and efficacy of DBS + Rehab and obtain marketing approval for this innovative treatment.
How does deep brain stimulation work in this context?
Deep brain stimulation involves surgical implantation of a device that sends electrical impulses to targeted areas of the brain, which can help improve motor function and support rehabilitation efforts.
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