For Patients and Caregivers

Advancing Neurological Care Through Research

At Central Texas Neurology Consultants, we are participating in numerous clinical trials aimed at transforming the future of neurological care. Our research team is deeply committed to advancing treatments in across a broad spectrum of neurological conditions including, Movement Disorders, Alzheimer's Disease, Neuromuscular, Sleep Disorders, and Multiple Sclerosis. By integrating clinical expertise with cutting-edge scientific inquiry, we strive to accelerate the development of therapies that improve patient outcomes and quality of life.

Currently Enrolling Studies

Why Take Part in Clinical Research?

Make a Difference

By taking part, you’re helping improve care for people with neurological conditions now and in the future. Your involvement brings us closer to better treatment options

Explore New Possibilities

Clinical studies may give you access to new therapies before they become widely available – and help you learn more about your condition

Receive Compensation

Many studies offer payment for your time and involvement, as well as coverage for certain related expenses

Powered by the Nira Medical Clinical Research Network

Central Texas Neurology Consultants is proud to be part of the Nira Medical Clinical Research Network – connecting us to leading research tools, proven practices, and the largest neurology-focused network in the country. With access to care innovations serving over 25,000 neurological patients nationwide, our physicians are helping to shape the future of treatment for neurological conditions.

Currently Enrolling Studies - Actively Seeking Participants With:

Parkinson's Disease
Mild Cognitive Impairment
Progressive Supranuclear Palsy
Myasthenia Gravis
Chronic Inflammatory Demyelinating Polyneuropathy
Spinal Muscular Atrophy
Movement Disorders
Alzheimer's Disease

Areas of Clinical Research Expertise

Memory Impairment
Essential Tremors
Neuromuscular Disorders
Epilepsy
Sleep Disorders
Headache

Participate in Clinical

Research

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Clinical Research Team

​Koni Lopez

​Study Coordinator
k.lopez@ctncpa.org

Sam Bruce 

​Study Coordinator

Mike Jaquez 

Pharmacist

Lenka Svedova

Clinical Research Coordinator

Hadie Mendoza

Clinical Research Assistant

Reina Suazo

Clinical Research Coordinator

Clinical Research 

Resources

Clinical Research FAQs

What Are Clinical Trials?

Clinical trials—also called research studies—are carefully designed studies that involve people. They help doctors and scientists learn more about health conditions and explore new ways to detect, treat, and prevent disease. People choose to join clinical trials to contribute to research, support future patients, and sometimes gain access to potential new treatments.Each study has a different purpose. Some focus on testing new medications, devices, or procedures, while others are observational and simply track health patterns or behaviors over time.

Are Clinical Trials Safe?

Safety is a top priority in all clinical trials. Every study is reviewed by an independent committee called an Institutional Review Board (IRB). This group—made up of doctors, scientists, and ethicists—ensures that the potential benefits outweigh the risks and that the study follows strict ethical guidelines.

Before joining, you’ll be fully informed about the study’s details, including any potential risks, so you can make the decision that’s right for you.

Why Join a Clinical Trial?

People take part in clinical research for many reasons. Some of the potential benefits include:

  • Access to investigational treatments before they’re widely available
  • Extra attention and care from experienced medical professionals
  • The chance to contribute to progress in care for people with similar conditions
What Does Participation Involve?

To join a clinical trial, you’ll first go through a screening process to see if the study is a good fit for you. This might include reviewing your medical history, doing lab tests, or having a physical exam.

You’ll also take part in something called “informed consent,” where the study team explains everything involved—including the purpose, time commitment, possible risks and benefits—so you can decide whether to join.

If you move forward, you’ll have regular check-ins with the study team. They’ll monitor how the treatment is working and how you’re feeling. A dedicated coordinator will help with scheduling, answer your questions, and make sure you’re supported every step of the way.

Things to Think About Before Joining

It’s important to ask questions and consider things like:

  • How long the study will last
  • What your participation will involve
  • If there’s a chance you’ll receive a placebo
  • The potential benefits and risks
  • Any travel or time away from daily routines
  • Whether your current treatment will change
  • If there are any costs—or if compensation is provided
We are in-network with all major insurance plans in the greater Central Texas area
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AriseHealth logoOE logo2020INC logoThe Paak logoEphicient logoToogether logoToogether logoToogether logoToogether logoToogether logoToogether logo
AriseHealth logoOE logo2020INC logoThe Paak logoEphicient logoToogether logoToogether logoToogether logoToogether logoToogether logoToogether logo
AriseHealth logoOE logo2020INC logoThe Paak logoEphicient logoToogether logoToogether logoToogether logoToogether logoToogether logoToogether logo