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Dystonia clinical trials

View clinical trials related to Dystonia.

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NCT ID: NCT00306865 Completed - Focal Dystonia Clinical Trials

Brain Changes in Patients With Focal Hand Dystonia

Start date: March 17, 2006
Phase: N/A
Study type: Observational

This study will examine how chemical changes in the brain produce symptoms of hand dystonia. Patients with dystonia have muscle spasms that cause uncontrolled twisting and repetitive movement or abnormal postures. In focal dystonia, just one part of the body, such as the hand, neck or face, is involved. The study will use positron emission tomography (PET) to find our which areas of the brain in patients with focal hand dystonia differ from healthy volunteers without focal hand dystonia. Healthy volunteers and patients with focal hand dystonia between 18 and 65 years of age may be eligible for this study. Candidates are screened with a medical history and physical and neurological examinations. Participants undergo the following procedures: - PET scanning: The PET scanner is shaped like a doughnut. The subject lies on a bed that can slide in and out of the scanner. A custom-molded plastic mask is placed on the face and head to support the head and prevent it from moving during scanning. Two radioactive substances - five doses (one per scan) of [15 O] water and one dose of [11C] flumazil are injected into the body through a vein. The dose of injected radioactive substance is very small, and they are not harmful to the body. The [15 O] water doses are injected during the first hour and scans are taken every 10 minutes. The [11C] flumazil is injected during the second hour. The radioactive substances are detected by the PET scanner and provide information on the functioning of the brain chemistry. - MRI scanning: MRI uses a magnetic field and radio waves to produce images of body tissues and organs. The patient lies on a table that is moved into the scanner (a narrow cylinder), wearing earplugs to muffle loud knocking and thumping sounds that occur during the scanning process. Scanning time for this study will be less than one hour. Subjects may be asked to lie still for up to 10 minutes at a time.

NCT ID: NCT00288509 Completed - Cervical Dystonia Clinical Trials

Open-label Extension Study of AbobotulinumtoxinA (Dysport®) for the Treatment of Cervical Dystonia

Start date: February 2006
Phase: Phase 3
Study type: Interventional

The aim of this study is to assess longer term safety and effectiveness of Dysport®.

NCT ID: NCT00285870 Completed - Dystonia Clinical Trials

Quantification of Upper Extremity Hypertonia

Start date: January 2006
Phase: N/A
Study type: Observational

Dr. Sanger and the research team want to learn about upper extremity hypertonia (stiffness) in children and young adults with cerebral palsy. Specifically, they want to learn about ways to measure the stiffness in the joints of hypertonic arms. The information the research team will collect includes any physical exams or computer generated data about your arm movements.

NCT ID: NCT00272246 Recruiting - Dystonia Clinical Trials

Bilateral Internal Pallidum Stimulation in Primary Generalized Dystonia

Start date: February 2005
Phase: Phase 2/Phase 3
Study type: Interventional

Primary generalized dystonia, also called idiopathic torsion dystonia or dystonia musculorum deformans is a disabling neurological condition which usually starts in childhood, mostly in a lower limb and spreads to other body parts as the disease progresses. Medical treatment is usually ineffective and most patients become wheelchair bound or even bedridden. Recently several case series and one RCT reported favourable results of bilateral deep brain stimulation (DBS) of the globus pallidus internus (GPi) for primary generalized dystonias. However, the number of patients treated with bilateral GPi stimulation is still limited. Therefore, we propose a RCT to investigate whether bilateral DBS of the GPi is an effective and safe treatment in patients with primary generalized dystonia.

NCT ID: NCT00257660 Completed - Cervical Dystonia Clinical Trials

Randomized, Placebo-Controlled Study of AbobotulinumtoxinA (Dysport®) for the Treatment of Cervical Dystonia

Start date: October 10, 2005
Phase: Phase 3
Study type: Interventional

The aim of this study is to demonstrate the effectiveness and safety of 500 units of Dysport manufactured at a new manufacturing facility in Europe.

NCT ID: NCT00210431 Completed - Cerebral Palsy Clinical Trials

Post Marketing Surveillance Study of Dysport

Start date: October 2004
Phase:
Study type: Observational

The purpose of this study is to provide further information regarding the risks and benefits of Dysport in marketed indications.

NCT ID: NCT00208091 Completed - Focal Dystonia Clinical Trials

Quantifying Musical Performance After Treatment With Myobloc in Musician's Dystonia

Start date: April 2003
Phase: Phase 4
Study type: Interventional

This study uses a computerized method of musical instrument digital interface (MIDI) quantification of performance before and after treatment with botulinum toxin type B (Myobloc ®, Solstice Neurosciences). Myobloc is a purified and diluted form of botulinum toxin used medically to relax unwanted muscle spasms and movements. The aim of the study is to determine the feasibility of quantifying change in performance following treatment.

NCT ID: NCT00178945 Completed - Cervical Dystonia Clinical Trials

Botulinum Toxin Type A (Botox) for the Treatment of Cervical Dystonia and Upper Thoracic Muscular Pain

Start date: March 2004
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to investigate the use of injections of Botox (botulinum toxin type A) for the treatment of chronic neck pain. Botox is an approved treatment for patients with cervical dystonia. Cervical dystonia is a chronic condition characterized by involuntary movements of the neck that are often painful. In this study, the response from Botox in patients with neck pain not associated with cervical dystonia will be compared to the pain response in patients with cervical dystonia.

NCT ID: NCT00169403 Recruiting - Dystonia Clinical Trials

Pallidal Stimulation in Patients With Idiopathic Generalised Dystonia

Start date: n/a
Phase: Phase 3
Study type: Interventional

Pallidal stimulation is effective in patients with generalised idiopathic dystonia. The aim of this study is to: 1. evaluate the efficacy and safety of this treatment in patients with idiopathic generalised dystonia, 3 years after surgery and 2. assess the recurrence of the motor symptoms after the switch off.

NCT ID: NCT00169338 Completed - Dystonia Clinical Trials

Pallidal Stimulation in Patients With Post-anoxic and Idiopathic Dystonia

Start date: September 2005
Phase: Phase 2
Study type: Interventional

Bilateral pallidal stimulation is effective in the treatment of patients with generalised idiopathic dystonia. The aim of this study is to evaluate the efficacy of bilateral pallidal stimulation in patients with post-anoxic generalised dystonia or non-generalised primary dystonia.