Expertise:

We offer a robust research program including many Clinical trials and innovative research for patients with Parkinson’s Disease and other movement disorders.

  • CAMELOT

    Principal Investigator:
    Sarah Horn, MD

     

     

    https://clinicaltrials.gov/study/NCT05590637

    Type of Study:
    Interventional/Randomized Control

    Summary
    The primary objective of this study is to determine whether treatment with pimavanserin or quetiapine is associated with a greater improvement in psychosis when used in a routine clinical setting to treat hallucinations and/or delusions due to Parkinson’s disease (PD) or dementia with Lewy bodies (DLB) – collectively referred to as Lewy body disease (LBD).

     

    Study Coordinator:
    Carolyn Paiz
    Office: 210-450-8830
    Email: paizc@uthscsa.edu

  • PD GENEration

     Principal Investigator:
    Okeanis Vaou, MD

     

     

    https://clinicaltrials.gov/study/NCT04994015

    Type of Study:
    Registry/ Observational

    Summary
    This study aims to retrospectively compare cases of SUDEP with matched control subjects cared for by the same epilepsy center to identify risk factors and potential biomarkers associated with SUDEP.

    Link to Sponsor’s Website:
    https://www.parkinson.org/advancing-research/our-research/pdgeneration

    Omalys Biggs Rodriguez

    Study Coordinator:
    Omalys Biggs
    Office: 210-450-8456
    Email: biggsrodrigu@uthscsa.edu

  • EXERCISE AND GAMING

    Principal Investigator:
    Anjali Sivaramakrishnan

     

     

    https://clinicaltrials.gov/study/NCT06133283

    Type of Study:
    Interventional

    Summary
    This study aims to determine the effects of aerobic exercise as a primer to add-on virtual reality (VR)-based rehabilitation on balance, postural control and neuroplasticity (ability of brain to adapt in structure and function) in individuals with Parkinson’s disease (PD). This study will utilize two groups – one group will receive the exercise and VR, while the other group will receive stretching exercise and VR over eight weeks. The study team will administer outcomes at baseline, post-intervention (8 weeks) and follow-up (6 weeks after post-assessment)

     

    Study Coordinator:
    Carolyn Paiz
    Office: 210-450-8830
    Email: paizc@uthscsa.edu

  • VERCISE-A4069

     Principal Investigator:
    Okeanis Vaou, MD

     

     

    https://clinicaltrials.gov/study/NCT02071134

    Type of Study:
    Registry/ Observational

    Summary
    The purpose of this registry is to compile characteristics of world-wide outcomes for the use of Boston Scientific’s commercially available Vercise DBS system in the treatment of Parkinson’s disease.  Subjects’ improvement in disease symptoms and overall Quality of life will be assessed during the study following DBS and compared with baseline. Additionally, the utilization of Image Guided Programming (IGP) when used as a planning tool for programming of patients is also evaluated

    Link to Sponsor’s Website:
    https://www.bostonscientific.com/en-US/search.html#q=vercise%20trial&first=10

    Study Coordinator:
    Carolyn Paiz
    Office: 210-450-8830
    Email: paizc@uthscsa.edu

  • ROSSINI

     Principal Investigator:
    Okeanis Vaou, MD

     

     

    https://clinicaltrials.gov/study/NCT06107426

    Type of Study:
    Observational

    Summary
    Parkinson’s disease (PD) is a neurological condition, which affects the brain.
    PD gets worse over time, but how quickly it progresses varies a lot from person to person. Some symptoms of PD are tremors, stiffness, and slowness of movement. The purpose of this study is to evaluate how effective ABBV-951 is in treating adult participants with advanced PD in real world setting.

     

    Study Coordinator:
    Carolyn Paiz
    Office: 210-450-8830
    Email: paizc@uthscsa.edu

  • SPARX3

     Principal Investigator:
    Okeanis Vaou, MD

     

     

    https://clinicaltrials.gov/study/NCT04284436

    Type of Study:
    Interventional/Randomized Control

    Summary
    This study is a Phase 3 multi-site, randomized, evaluator-masked, study of endurance treadmill exercise on changes in the Movement Disorder Society-Unified Parkinson Disease Rating Scale (MDS-UPDRS) Part III score at 12 months among persons with early stage Parkinson disease. 370 participants will be randomly assigned to 2 groups: 1)60-65% HRmax or 2)80-85% HRmax 4 times per week. The primary objective is to test whether the progression of the signs of Parkinson’s disease is attenuated at 12 months in among persons who have not initiated medication for Parkinson Disease (PD) when they perform high-intensity endurance treadmill exercise.

    Link to Sponsor’s Website:
    https://www.sparx3pd.com/home/volunteer

     

    Study Coordinator:
    Carolyn Paiz
    Office: 210-450-8830
    Email: paizc@uthscsa.edu