Neurologic Disorders Clinical Trials

This is an open-label trial. All NMO or NMO Spectrum Disorder (NMOSD) patients who have completed the double-blind, randomized, placebo-controlled ECU-NMO-301 (PREVENT) trial may be eligible to participate in this extension trial. Prior to initiating any extension trial procedures, an informed consent form must be signed and inclusion/exclusion criteria must ...

The Medtronic Sofamor Danek USA, Inc. CD HORIZON® LEGACY™ PEEK Rod Spinal System is currently marketed in both the US and EU and is designed to treat conditions of the lumbar spine as supplemental fixation for interbody fusion. The rods are made of polyetheretherketone (PEEK) with titanium tips or tantalum ...

The purpose of this study is to collect retrospective real-world clinical data to assess the performance including efficacy and safety of CD HORIZON® LEGACY™ PEEK Rod Spinal System used as supplemental fixation for a posterior interbody fusion cage in subjects who have undergone a posterior non-cervical spinal fusion procedure for ...

Study for Pediatric ADHD Learning that your 4 or 5 year old child has attention-deficit/hyperactivity disorder (ADHD) is challenging. It may leave you wondering what options are available for your child and whether they will be safe for your child at such a young age. New clinical research studies will ...

Study for Pediatric ADHD Learning that your [4 to 12] [4 or 5] year old child has attention-deficit/hyperactivity disorder (ADHD) is challenging. It may leave you wondering what options are available for your child and whether they will be safe for your child at such a young age. New clinical ...

A clinical trial seeking patients for a research study for the treatment of Essential Tremor.

We are studying patients with paraneoplastic neurologic disorders (The Hu syndrome, a.k.a. Paraneoplastic Subacute Sensory Neuropathy/Encephalomyelitis or Limbic Encephalopathy, and The Ri Syndrome, a.k.a. Paraneoplastic Opsoclonus-Myoclonus Ataxia) in two IRB-approved protocols at the Rockefeller University Clinical Research Center. One study is aimed at furthering our understanding of the cause of ...

The purpose of this study is to assess the safety and tolerability of pimavanserin compared to placebo in adult and elderly subjects with neuropsychiatric symptoms related to neurodegenerative disease.

The purpose of the PSR platform is to provide continuing evaluation and periodic reporting ofsafety and effectiveness of market-released products for their intended use. PSR data will support post-market surveillance activities initiated by Medtronic and post-approval studies directed by a government and/or a regulatory authority. Conducting product surveillance in large ...

A Trial Evaluating the Efficacy, Safety, & Tolerability of Centanafadine Sustained-release Tablets in Adults With Attention-deficit/Hyperactivity Disorder