Tourette Syndrome Clinical Trial
Official title:
Evaluation of Tourette's Syndrome With Multimetabolite H-Magnetic Resonance Spectroscopy at 3T
This study will use magnetic resonance imaging (MRI) and magnetic resonance spectroscopy
(MRS) of the brain to try to gain a better understanding of the disease process in Tourette s
syndrome, a neuropsychiatric disorder characterized by motor and vocal tics. Tourette s
syndrome is also associated with behavioral and emotional disturbances, including symptoms of
attention deficit hyperactivity disorder (ADHD) and obsessive-compulsive disorder (OCD). MRI
and MRS show chemical substances in the brain. Findings in normal volunteers will be compared
with those of patients.
Healthy volunteers and patients with Tourette s syndrome 14 years of age and older may be
eligible for this study. Volunteers will be screened with a medical history and physical and
neurological examinations. Patients will be screened through NINDS protocol 93-N-0202.
Participants will undergo MRI and MRS. MRI uses a strong magnetic field and radio waves to
visualize brain anatomy and chemistry. For this study, the subject lies on a stretcher, which
is moved into a strong magnetic field (the MRI scanner). Earplugs are worn to muffle loud
thumping noises caused by the electrical switching of the radio frequency circuits. During
the study, the subject lies still during each scan, for 1 to 8 minutes at a time. Total
scanning time varies from 20 minutes to 2 hours, with most examinations lasting between 45
and 90 minutes. The subject can speak through an intercom with the staff member performing
the study at all times during the procedure. Up to 5 studies may be performed.
OBJECTIVE
The purpose of this study is to obtain a better understanding of the pathophysiology of
Tourette's Syndrome (TS) with nuclear magnetic spectroscopic imaging. The basal ganglia have
been implicated in the origin of tics, and we plan to use spectroscopy to determine whether
there is any neuronal degeneration or a decrease in aminobutyric acid (GABA) within the basal
ganglia, thalamus, or frontal cortex of patients with TS when compared to normal individuals.
STUDY POPULATION
This research will be conducted using patients with TS and normal volunteers.
DESIGN
Patients and normal volunteers will be scanned with 3 Tesla General Electric (GE) magnetic
resonance imager using magnetic resonance spectroscopy (MRS) to measure N-acetylaspartate,
choline, creatine, lactate and GABA.
OUTCOME MEASURES
Concentrations of metabolites will be compared between two groups.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT04851678 -
Longitudinal Impact of Stressors in Adults With Tourette Syndrome
|
||
Completed |
NCT02605902 -
Trial to Demonstrate the Efficacy and Safety of Internet-delivered Behavioral Treatment for Adults With Tic Disorders
|
N/A | |
Completed |
NCT04007913 -
Incorporating teleCBIT Into a Hospital-Based Tic Program
|
N/A | |
Completed |
NCT02900144 -
Modified Comprehensive Behavioral Intervention for Tics (M_CBIT)
|
N/A | |
Completed |
NCT02256475 -
Safety, Pharmacokinetics, and Pharmacodynamics of NBI-98854 in Children and Adolescents With Tourette Syndrome
|
Phase 1 | |
Completed |
NCT02216474 -
Brain Stimulation in Movement Disorders
|
N/A | |
Completed |
NCT01329198 -
Brain Stimulation for the Treatment of Tourette Syndrome
|
N/A | |
Terminated |
NCT00952601 -
Pilot Study of the Modified Atkins Diet for Tourette Syndrome
|
Phase 1 | |
Enrolling by invitation |
NCT00355927 -
Sedation During Microelectrode Recordings Before Deep Brain Stimulation for Movement Disorders.
|
N/A | |
Completed |
NCT00206323 -
A Randomized, Placebo-controlled, Tourette Syndrome Study.
|
Phase 3 | |
Completed |
NCT00004376 -
Phase III Randomized, Double-Blind, Placebo-Controlled Study of Guanfacine for Tourette Syndrome and Attention Deficit Hyperactivity Disorder
|
Phase 3 | |
Completed |
NCT04498364 -
Extinction Learning in Adults With Tourette Syndrome
|
N/A | |
Completed |
NCT00755339 -
Role of the Sensory Experience in Generating Motor Tics in Tourette Syndrome
|
||
Completed |
NCT03325010 -
Safety, Tolerability, and Efficacy of NBI-98854 for the Treatment of Pediatric Subjects With Tourette Syndrome
|
Phase 2 | |
Not yet recruiting |
NCT06081348 -
Sertraline vs. Placebo in the Treatment of Anxiety in Children and AdoLescents With NeurodevelopMental Disorders
|
Phase 2 | |
Completed |
NCT01702077 -
Neurofeedback for Tourette Syndrome
|
N/A | |
Completed |
NCT01719523 -
Open-Trial of EPI-743 for Adults With Tourette Syndrome
|
Phase 1 | |
Completed |
NCT00231985 -
Effectiveness of Behavior Therapy and Psychosocial Therapy for the Treatment of Tourette Syndrome and Chronic Tic Disorder
|
Phase 2 | |
Completed |
NCT00206336 -
An Open-label Study to Determine the Efficacy and Safety of Topiramate in the Treatment of Tourette Syndrome.
|
Phase 3 | |
Terminated |
NCT03732534 -
Rollover Study for Continuing NBI-98854 Administration in Pediatric Subjects With Tourette Syndrome
|
Phase 2 |