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Dystonia clinical trials

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NCT ID: NCT02509338 Terminated - Tardive Dystonia Clinical Trials

Validation of the Implantation of a New Electrode for the Treatment of Dystonia

MONOCONTACT
Start date: October 2013
Phase: N/A
Study type: Interventional

The main objective of the trial is to study the technical feasibility of the implantation of a new electrode Monocontact deep brain stimulation electrode in dystonia.

NCT ID: NCT02106936 Terminated - Healthy Volunteers Clinical Trials

Depotentiation in People With Focal Hand Dystonia

Start date: March 5, 2014
Phase: N/A
Study type: Observational

Background: - Focal hand dystonia (FHD) causes muscles to contract, leading to abnormal movements or postures. Musicians, writers, and athletes often get it. Researchers want to study how patients with this condition learn, a process of the brain that depends on a property called plasticity. Objective: - To study brain plasticity in people with FHD. Eligibility: - Right-handed adults 18 years and older with FHD. - Healthy, right-handed adult volunteers. Design: - Participants will be screened with medical history, physical exam, pregnancy test, and questionnaire about their right-handedness. - Participants will have 2 study visits on 2 different days. - Participants will sit in a chair and have up to 30 Transcranial Magnetic Stimulation (TMS) pulses on the left side of the head. A brief electrical current passes through a wire coil on the scalp. They will hear a click and may feel a pulling on the skin or muscle twitches. They may have to keep their eyes open and remain alert, tense certain muscles, or perform simple finger movements. - Forty more pulses, with 10 seconds between, will be given on the left side of the head. Some will be small, some big. - Researchers will measure muscle response through small electrodes taped to the right hand. - A cloth cap will be put on the participant s head. Researchers will write on tape on the cap. - Participants will have the r-PAS. An electrical stimulator will be placed on the nerve at the right wrist. Repeated magnetic pulses will be delivered in trains or short bursts together with electrical stimulation of nerve. Participants will receive up to 840 pulses. - Participants will be contacted after a few days for a follow-up check.

NCT ID: NCT01792336 Terminated - Dystonia Clinical Trials

Transcranial Magnetic Stimulation for Focal Hand Dystonia

Start date: February 13, 2013
Phase:
Study type: Observational

Background: - The brain has natural electrical rhythms of brain activities. These rhythms may be different in people with movement disorders, such as dystonia (involuntary muscle movement, cramps, or tremors). Understanding these rhythms may provide more information about movement disorders. - Focal hand dystonia, also known as "writer's cramp" or "musician's cramp," is a painful condition that affects the hand and arm muscles. Researchers want to use transcranial magnetic stimulation (TMS) to study brain rhythms in people with and without focal hand dystonia. Objectives: - To better understand brain rhythms involved in focal hand dystonia. Eligibility: - Individuals between 18 and 70 years of age who are right-handed and have focal hand dystonia. - Healthy right-handed volunteers between 18 and 60 years of age. Design: - Participants will be screened with a physical exam and medical history. - This study includes two tests: a pilot test and a main test. The pilot test will determine the frequency of TMS that will be used in the main test. Participants may be in one or both tests. Each test requires a single outpatient visit that will last up to 5 hours. - Participants will have a base test to see how their muscles respond to TMS. This will look at the electrical activity of the muscles. Participants will have a wire coil held on their scalp. A brief electrical current will pass through the coil. It creates a magnetic pulse that stimulates the brain. Researchers will test the TMS on the right and left sides of the head. This will help find the spot that activates the finger muscles, and see how much TMS is needed. - In the main test, participants will have repetitive TMS (rTMS). rTMS involves repeated magnetic pulses delivered in short bursts. There will be four pulses in each burst. Participants will have multiple bursts during the test. This test will look at how the muscles of the hand and fingers respond to brain stimulation. - Treatment for focal hand dystonia will not be provided as part of this study.

NCT ID: NCT01750346 Terminated - Focal Dystonia Clinical Trials

Acetyl Hexapeptide-8 for Blepharospasm

Start date: November 2012
Phase: Phase 2
Study type: Interventional

Background: - Blepharospasm is caused by excessive contraction of the muscles that close the eye. One treatment is botulinum neurotoxin (BoNT), which works by weakening those muscles. Like BoNT, acetyl hexapeptide-8 (AH-8) works to weaken the muscles, but is available as a skin cream. AH-8 is the active ingredient in a number of cosmetic creams used to treat wrinkles. Researchers thought that AH-8 cream could be used to treat blepharospasm, but the original dose studied was not very effective. They want to try a higher dose of AH-8 in a cream to see if it can be a more effective treatment. Objectives: - To see if AH-8 cream can improve the symptoms of blepharospasm. Eligibility: - Individuals at least 18 years of age who have blepharospasm that is severe enough to require treatment. Design: - This study will involve up to eight study visits. - Participants will be screened with a physical exam and medical history. They will answer questions about their symptoms. They will also have a blink test to see how severe the blepharospasm is. At this visit, participants will receive one of three types of cream. One cream will have a low dose of AH-8, one will have a higher dose of AH-8, and the other will be a placebo (no AH-8). - One month later, participants will have a followup visit, with tests similar to the first visit. They will also receive more of the cream. - One month later, participants will have another visit with the same tests. They will be videotaped at this visit to study their facial movements. Those who have responded to the treatment will continue to use the cream. Those who have not responded will be offered the chance to have BoNT injections, and will stop taking the cream. - One month later, participants who had BoNT injections will have a final visit to check for possible side effects. Those who continued to take the cream will continue on the study. - The fifth and sixth visits will involve the same tests as before. At the seventh visit, remaining participants will be offered the chance to have BoNT injections, and will stop taking the cream. - The final visit will check for any side effects from the cream or the injections.

NCT ID: NCT01191307 Terminated - Epilepsy Clinical Trials

Assess Specific Kinds of Children Challenges for Neurologic Devices Study

Start date: March 2009
Phase: N/A
Study type: Observational

The ASK CHILDREN study is intended to aid in future development of various neurologic devices (i.e. neuroprostheses). The ASK CHILDREN study seeks to use study information obtained to identify more efficient strategies in the evaluation and review of neuroprostheses regulated by the Agency.

NCT ID: NCT01105845 Terminated - Movement Disorders Clinical Trials

Genetics of Motor Learning

Start date: April 14, 2010
Phase:
Study type: Observational

Background: - New studies in human genetics have revealed information about genetic connections to memory and motor behavior. Researchers are interested in investigating the role of genetics in motor learning, in conjunction with related studies taking place in the Human Motor Control Section of the National Institute of Neurological Diseases and Stroke (NINDS). Participants in motor learning studies conducted at NINDS will be asked to provide blood samples for further evaluation. Objectives: - To create a repository of blood samples from patients and healthy subjects who are participating in NINDS motor learning studies. Eligibility: - Individuals between 18 and 100 years of age who are or will be participating in motor learning research studies at the National Institutes of Health. Design: - Blood draws for genetic testing will usually be done on the same day as the motor learning study. Participants will provide one blood sample for research. - No treatment will be provided under this study....

NCT ID: NCT00895063 Terminated - Dystonia Clinical Trials

Effect of Vocal Exercise After Botulinum Toxin Injection for Spasmodic Dysphonia

Start date: December 2007
Phase: N/A
Study type: Interventional

Studies have suggested that voluntary muscle exercise in the hand and face after botulinum toxin injection may enhance the clinical effects of the toxin. Exercise may speed up the absorption of the toxin by the nerves and enhance the clinical response. This study will explore the effect of exercise on botulinum toxin injections for spasmodic dysphonia (SD).

NCT ID: NCT00760318 Terminated - Cervical Dystonia Clinical Trials

Keppra for Cervical Dystonia

Keppra
Start date: November 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate if there is an improved response in CD symptoms when Keppra is used as adjunctive therapy to Botox.

NCT ID: NCT00506012 Terminated - Myoclonus Clinical Trials

Pilot Efficacy Study of T2000 in Myoclonus Dystonia

Start date: August 2007
Phase: Phase 2
Study type: Interventional

This pilot study will evaluate the safety and efficacy of once daily T2000 when used to treat patients with Myoclonus Dystonia over a 12 week period.

NCT ID: NCT00487383 Terminated - Dystonia Clinical Trials

Brain Changes in Blepharospasm

Start date: June 12, 2007
Phase:
Study type: Observational

This study will examine the role of certain areas of the brain in blepharospasm, a type of dystonia (abnormality of movement and muscle tone) that causes unwanted or uncontrollable blinking or closing of the eyelids. The study will compare brain activity in healthy volunteers and in people with blepharospasm to find differences in the brain that may lead to better treatments for dystonia. Healthy volunteers and people with blepharospasm who are 18 years of age and older may be eligible for this study. All candidates are screened with a medical history. People with blepharospasm also have a physical examination and blepharospasm rating. Participants undergo transcranial magnetic stimulation (TMS) and electromyography (EMG) in two 4-hour sessions, separated by 1 to 7 days. TMS A wire coil is held on the subject s scalp. A brief electrical current is passed through the coil, creating a magnetic pulse that stimulates the brain. The subject hears a click and may feel a pulling sensation on the skin under the coil. There may be a twitch in muscles of the face, arm or leg. During the stimulation, subjects may be asked to tense certain muscles slightly or perform other simple actions. Repetitive TMS involves repeated magnetic pulses delivered in short bursts of impulses. Subjects receive 60 pulses per minute over 15 minutes. EMG Surface EMG is done during TMS to measure the electrical activity of muscles. For this test, electrodes (small metal disks) are filled with a conductive gel and taped to the skin of the face.