SFM Clinical Research, LLC is an independent research company specializing in the conduction of clinical trials for neurological disorders. Founded by board certified neurologists with decades of experience, our team is committed to bridging the gap between standard practice and innovative therapies. The wellbeing of our patients is our number one priority and we pride ourselves on maintaining a high standard of care to ensure the ethical conduction of each clinical trial.

For more information or to be evaluated for clinical trial entry, please call 561-939-0333

We are recruiting for clinical studies!

Do you suffer from one of the following?

• Alzheimer's Disease
• Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
• Neurogenic Orthostatic Hypotension
• Multiple Sclerosis
• Myasthenia Gravis
• Migraines
  
  

FAQs

What is a clinical trial?
Before a therapy is approved as standard of care it must first undergo a trial period. A clinical trial is a method in which clinical researchers evaluate a medical, surgical or behavioral intervention. The data collected during a clinical trial is used to determine whether a therapy is safe and effective against a specific medical condition. Qualified physicians, research professionals, and an Institutional Review Board (IRB) overlook clinical trials to ensure the ethical conduction of clinical research.

What happens during a clinical trial?
Once the participant is deemed a potential candidate, the Informed Consent is reviewed in depth with the participant and/or legally authorized representative (LAR). Study procedures will only begin upon receipt of voluntary consent from the participant and/or LAR in the form of a signature and date on the Informed Consent Form. After the Informed Consent process, the participant may undergo a screening period in which preliminary study procedures are performed to confirm study eligibility. A team of healthcare professionals will provide detailed guidance for participating in the trial, monitor the participant closely during the trial, and communicate with the participant after trial completion. It is important to note that participation in any clinical trial is completely voluntary and that consent may be withdrawn by the participant and/or LAR at any time.

What is Informed Consent?
Informed Consent is the process in which the participant and/or legally authorized representative (LAR) voluntarily provide consent to participate in a clinical trial. Prior to providing consent, the participant is given the opportunity to review all study-related information and address all questions and concerns with the research team and healthcare provider. It is important to note that participation in any clinical trial is completely voluntary and that consent may be withdrawn by the participant and/or LAR at any time.