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Role of Dopamine Receptors in Primary Focal Dystonias

Role of Dopamine Receptors in Primary Focal Dystonias

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01373840
Enrollment
40
Registered
2011-06-15
Start date
2011-09-30
Completion date
2016-04-30
Last updated
2018-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Focal Dystonias, Healthy

Keywords

focal, dystonia, dopamine, receptor

Brief summary

Dystonia is a disabling movement disorder characterized by repetitive patterned or sustained muscle contractions causing twisting or abnormal postures that may afflict 250,000 people in the U.S. While the pathophysiology of dystonia remains uncertain the treatment is rather rudimentary. A better understanding of neural mechanisms of dystonias is not only an invaluable prerequisite for developing better treatment options but also a step toward better understanding of the complex network of basal ganglia. In this study I will investigate if there is any difference between the dopamine receptors and dopamine in people with dystonia and healthy subjects.

Interventions

None listed

Sponsors

National Institute of Neurological Disorders and Stroke (NINDS)
CollaboratorNIH
Washington University School of Medicine
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age \>20 * Male or Female * Any race or ethnicity * Primary focal dystonia (arm or cranial) * Ability to give informed consent

Exclusion criteria

* Family history of dystonia * Pregnancy (confirmed with negative urine pregnancy test in women of child bearing potential), breastfeeding * Exposure to radiation therapy * Any MRI contraindications such as foreign metallic implants, pacemaker, and aneurysm clip etc. * History of cardiac disease, uncontrolled hypertension, abnormal EKG during screening phase * History of exposure to any drugs affecting dopaminergic systems within the last 6 months (e.g. dopamine receptor blocking agents, cocaine, amphetamine, tetrabenazine, reserpine, L-dopa, dopamine agonists, as they might affect the dopamine receptor binding or endogenous dopamine). * Active depression (Beck Depression Inventory\_II \>14) * Cognitive impairment (Mini-Mental State Score \<27) * CNS active medications such as gabapentin or narcotics, muscle relaxants which might be given for pain in the 3 days prior to study * History of stroke, seizure, cerebral palsy, generalized dystonia, parkinsonism, inability to hold head still during the scanning time.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026