Recruiting Studies
Advanced SearchData: ClinicalTrials.gov · Source of record for eligibility and locations
Top Cities for Tourette Syndrome Clinical Trials
Tourette Syndrome clinical trials are recruiting across 25 cities. Here are the cities with the most active studies:
Tourette Syndrome Trial Phases
16 research organizations are sponsoring tourette syndrome trials.
About Tourette Syndrome
Tourette syndrome is a neurological disorder characterized by repetitive, involuntary movements and vocalizations called tics. It typically appears in childhood and often improves in adulthood. Treatment includes behavioral therapy and medications for severe tics.
Clinical trials are advancing new treatments for tourette syndrome. Currently, 20 studies are recruiting a combined 4,915 participants across the United States. Research is being conducted by 16 organizations including University of Pittsburgh, National Institute of Environmental Health Sciences (NIEHS), Mayo Clinic and 13 others.
2026 Tourette Syndrome Research Landscape
As of July 2026, the tourette syndrome clinical trial landscape includes 20 actively recruiting studies across 25 cities in the United States. These studies are collectively seeking 4,915 participants, with an average enrollment target of 246 per study.
The research spans multiple phases of development: 10 studies are in NA.
Research is being led by 16 different organizations, including University of Pittsburgh, National Institute of Environmental Health Sciences (NIEHS), Mayo Clinic, The Hospital for Sick Children, Vanderbilt University Medical Center, and 11 others. The large number of sponsors reflects significant research interest and investment in tourette syndrome treatment advancement.
Geographically, tourette syndrome trials are most concentrated in Pittsburgh, Pennsylvania (2 trials); Los Angeles, California (2 trials); Boston, Massachusetts (2 trials); New Haven, Connecticut (2 trials); Nashville, Tennessee (2 trials) and 7 other cities.
Featured Tourette Syndrome Studies
Highlighted recruiting studies for tourette syndrome, selected by enrollment size and research scope.
Neurogenetics Patient Registry
The objective of this project is to develop a Neurogenetics patient database and bio repository - which includes clinical information regarding history, physical examination, laboratory testing including genetic testing (NextGen sequencing including whole exome and whole genome sequencing, SNParray, etc.), neuroradiology studies, neurophysiology studies - all ordered as clinically deemed appropria...
Inherited Reproductive Disorders
Background: \- During puberty, children begin to develop into adults. Problems with the hormones released during puberty can affect the reproductive system. Some people have low hormone levels that severely delay or prevent puberty. Others start puberty abnormally early. Other people may have a normal puberty but develop reproductive disorders later in life. Researchers want to study people with ...
Clinical and Molecular Characteristics of Histiocytic Disorders
This study is being done to collect medical and personal histories as well as a samples of blood, other body fluid and/or tumor/disease tissue for current and future research studies on histiocytic disorders.
Frequently Asked Questions About Tourette Syndrome Clinical Trials
Are there tourette syndrome clinical trials near me?
Yes, there are 20 tourette syndrome clinical trials currently recruiting across 25+ cities in the United States, including Pittsburgh, Pennsylvania; Los Angeles, California; Boston, Massachusetts. Browse the studies above to find one at a location convenient for you.
How do I join a tourette syndrome clinical trial?
To join a tourette syndrome clinical trial: 1) Browse the available studies on this page, 2) Click on a study that interests you, 3) Check the study locations to find a site near you, 4) Review the eligibility criteria, and 5) Contact the study site or complete the eligibility form. The process is free and you can withdraw at any time.
Are tourette syndrome clinical trials free?
Yes, participation in tourette syndrome clinical trials is free. Study-related treatments, medical tests, and doctor visits are provided at no cost to participants. Many studies also offer compensation for your time and travel expenses.
What types of tourette syndrome treatments are being studied?
Current tourette syndrome clinical trials are testing a range of approaches across NA (10 studies). These include new drugs, combination therapies, medical devices, and other interventions sponsored by 16 research organizations.
Is it safe to participate in tourette syndrome clinical trials?
Clinical trials are carefully regulated by the FDA and institutional review boards (IRBs). All trials must follow strict safety protocols, and participants receive close medical monitoring throughout the study. You can withdraw from a trial at any time without penalty.
Data updated July 16, 2026 from ClinicalTrials.gov
About This Data
Data: ClinicalTrials.gov · Source of record for eligibility and locations
Clinical trial information on this page is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health (NIH) and National Library of Medicine (NLM). Study data is refreshed every hour to ensure accuracy.
Medical Disclaimer: The information provided on this page is for informational purposes only and does not constitute medical advice. Always consult with a qualified healthcare provider before making decisions about clinical trial participation or changes to your treatment plan.
Page reviewed by the HelloStudys Research Team · Last updated July 16, 2026 · Data from ClinicalTrials.gov