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Dystonic Disorders clinical trials

View clinical trials related to Dystonic Disorders.

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NCT ID: NCT03409120 Completed - Parkinson Disease Clinical Trials

Unlocking Dystonia From Parkinson's Disease With Directional DBS Technology

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

This study occurs during five visits that are already scheduled as part of "Biomarkers to Guide Directional DBS for Parkinson's Disease" (ClinicalTrials.gov Identifier: NCT03353688). If participants have dystonia associated with Parkinson's disease, the investigators will consent and administer one additional rating scale (Burke-Fahn-Marsden Dystonia Rating Scale) to assess the severity of dystonia.

NCT ID: NCT03381456 Completed - Dystonia, Primary Clinical Trials

Task-dependent Operation of a Mechanism Intracortical Inhibition in Dystonia

LICIdystonie
Start date: April 2015
Phase: N/A
Study type: Interventional

Cortical excitability depends on inhibitory mechanisms efficiency among which long latency intracortical inhibition (LICI) can be studied by paired pulses transcranial magnetic stimulation (TMS). Some recent evidences suggest that LICI may be one of the mechanisms by which the motor comment is adapted to the ongoing motor task with LICI strength being dependent on task complexity. In writer cramp and musician cramp, two forms of dystonia, the cortical excitability is not correctly modulated in some complex gestures. the hypothesis is that this task dependent perturbation of excitability in writer cramp could be due to a lack of LICI efficiency.

NCT ID: NCT03380676 Completed - Dysphagia Clinical Trials

Study of Speech Disorders , Voice and Swallowing in Primary Dystonia Oromandibular

DOM
Start date: February 2014
Phase: N/A
Study type: Observational

To better define the clinical characteristics of oromandibular dystonia, we aimed to study voice, speech and swallowing disorders in idiopathic oromandibular We planned to include consecutive patients followed in Lille Movement disorders department for idiopathic oromandibular dystonia and matched, healthy control subjects. Voice and speech disorders had to be assessed with the phonetic analysis, perceptive analysis and motor examination modules of the "Batterie d'Evaluation Clinique de la Dysarthrie" (Clinical Evaluation of Dysarthria), the Grade, Rough, Breathy, Asthenic, Strained scale, and a computer recording. Activities of daily living had to be assessed with the Oromandibular Dystonia Questionnaire, the Voice Handicap Index and the Deglutition Handicap Index.

NCT ID: NCT03369613 Completed - Clinical trials for Primary Cervical Dystonia

Transcranial Electrical Stimulation for Cervical Dystonia

Start date: October 27, 2017
Phase: N/A
Study type: Interventional

There are two phases. Phase I: A single visit which includes a screening, clinical scales, and a MRI scan with simultaneous tES/sham tES in a randomized block design. Enrolls both Cervical Dystonia (CD) patients and healthy controls. Phase II: 5 consecutive days of 30-90 min visits to campus for tES or sham tES. Transcranial magnetic stimulation (TMS) measures and clinical scales will also be included on Day 1 and Day 5 visits. Enrolls only CD patients.

NCT ID: NCT03363113 Completed - Dystonia; Orofacial Clinical Trials

Outcome of Botulinum Toxin Treatment for Oromandibular Dystonia

rétroBODOM
Start date: January 1, 2016
Phase: N/A
Study type: Observational

Symptoms of oromandibular dystonia can be alleviated by injections of botulinum toxin. The scope of this study is to describe the efficacy of this procedure, by a retrospective systematic review of patients medical charts

NCT ID: NCT03347240 Completed - Secondary Dystonia Clinical Trials

Neuroablation Versus Neuromodulation Techniques for Treatment of Secondary Dystonia

Start date: December 1, 2013
Phase: N/A
Study type: Interventional

The disability inflected by dystonia encouraged the development of many neurosurgical procedures. This is a prospective study included 120 patients suffering from intractable secondary dystonia. They were subjected to different neurosurgical treatments and were assessed through the follow up period

NCT ID: NCT03318120 Completed - Dystonia Clinical Trials

Exercise Training in Dystonia

Start date: November 6, 2017
Phase: N/A
Study type: Interventional

The purpose of this research study is to investigate how the brain and motor behavior changes in individuals with dystonia and other involuntary movement disorders and healthy individuals over time with exercise training.

NCT ID: NCT03307161 Completed - Parkinson Disease Clinical Trials

Osteopathic Manual Treatment Parkinson's Disease and Truncal Dystonia

Start date: November 2016
Phase: N/A
Study type: Interventional

This study will determine if posture and heart rate variability will significantly improve in Parkinsons disease with camptocormia after osteopathic manual treatments dystonia.

NCT ID: NCT03232320 Completed - Dystonia Clinical Trials

Meditoxin® Treatment in Patients With Cervical Dystonia

Start date: July 6, 2017
Phase: Phase 3
Study type: Interventional

To determine the efficacy and safety of Meditoxin in subjects with cervical dystonia compared with placebo (normal saline)

NCT ID: NCT03223623 Completed - Dystonia Clinical Trials

Pathophysiology of Focal Hand Dystonia

Start date: December 12, 2017
Phase: N/A
Study type: Interventional

Background: Little is known about the problems in brain function in focal hand dystonia (FHD) or complex regional pain syndrome (CRPS) dystonia. It is unclear why some CRPS patients develop dystonia but others do not. Researchers want to learn which area of the brain is involved in CRPS dystonia compared with FHD. Objectives: To understand why people with CRPS develop dystonia, and if these reasons are different in people with FHD. Eligibility: Adults ages 18 - 70 with CRPS dystonia OR with CRPS without dystonia OR with FHD and Healthy volunteers of similar age. Design: Participants will be screened with physical exam, neurological exam, and medical history. They may give a urine sample and will answer questions. Participants can have 4 - 5 outpatient visits or stay at the clinical center for approximately 5-6 days. Participants will have MRI scans. They will lie on a table that slides in and out of a scanner that takes pictures of their brain. They will do small tasks or be asked to imagine things during the scanning. Participants will have transcranial magnetic stimulation (TMS) sessions for a few hours, with breaks. A brief electrical current passing through a well insulated wire coil on the scalp creates a magnetic pulse. This affects brain activity. Participants may do small tasks during TMS. Participants will have the electrical activity of their muscles measured during TMS sessions. Small sticky pads will be attached to their hands and arms. Participants ability to feel 2 separate stimuli as different will be tested by using a weak electrical shock to their fingers. They will also be asked to feel small plastic domes with ridges, that may cause discomfort.