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Dyskinesias clinical trials

View clinical trials related to Dyskinesias.

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NCT ID: NCT03606200 Recruiting - Clinical trials for Primary Ciliary Dyskinesia

Swiss Primary Ciliary Dyskinesia Registry

CH-PCD
Start date: January 2013
Phase:
Study type: Observational [Patient Registry]

The Swiss Primary Ciliary Dyskinesia (PCD) Registry is a national patient registry that collects information on diagnosis, symptoms, treatment and follow-up of patients with PCD in Switzerland and provides data for national and international monitoring and research.

NCT ID: NCT03568487 Recruiting - Scapular Dyskinesis Clinical Trials

Scapula Adaption in Overhead Athletes

Start date: January 2, 2019
Phase: N/A
Study type: Interventional

Previous studies have proposed various ways to assess scapular dyskinesis, but they were impractical in clinical setting or the validity was questioned. The novel scapulometer we developed can measure the prominence of scapular medial border and inferior angle. We would like to examine its reliability and validity in subjects with symptomatic scapular dyskinesis. The long-term, high-intensity, unilateral loading may cause overhead athletes to develop adaptive changes in shoulder kinematics, range of motion (ROM) and strength in the dominant arm. We hypothesized that these changes may be related to scapular dyskinesis. According to the previous studies, we expect electromyography (EMG) biofeedback training can help improve the ratio of muscle activation of scapular muscle.

NCT ID: NCT03531060 Completed - Parkinson Disease Clinical Trials

A Clinical Study of IRL790 in Patients With Parkinson's Disease Experiencing Levodopa Induced Dyskinesia

Start date: November 8, 2016
Phase: Phase 1/Phase 2
Study type: Interventional

This is a Phase 1b study investigating the safety and tolerability of IRl790 as adjunct therapy in patients with Parkinson disease. IRL790/placebo is taken for 28 days.

NCT ID: NCT03517865 Recruiting - Clinical trials for Primary Ciliary Dyskinesia

International Primary Ciliary Dyskinesia Cohort

iPCD
Start date: January 2013
Phase:
Study type: Observational

The iPCD Cohort is an international cohort that assembles available retrospective datasets and prospectively newly collected clinical and diagnostic data from patients suffering from primary ciliary dyskinesia (PCD) worldwide, to answer pertinent questions on clinical phenotype, disease severity, prognosis and effect of treatments in patients with this rare multiorgan disease.

NCT ID: NCT03497013 Completed - Tardive Dyskinesia Clinical Trials

Effect of tDCS on Cognition, Symptoms in Chronic Schizophrenia Patients With Tardive Dyskinesia

Start date: July 31, 2017
Phase: N/A
Study type: Interventional

The aim of the study was to evaluate the efficacy, safety, and cognitive function of transcranial direct current stimulation (tDCS) in chronic schizophrenia patients with tardive dyskinesia (TD).

NCT ID: NCT03495024 Recruiting - Schizophrenia Clinical Trials

Smoking Cessation With Varenicline in Schizophrenia: Antipsychotic-Induced Neurological Symptoms as Correlates

Start date: January 1, 2019
Phase: Phase 4
Study type: Interventional

To test the feasibility of studying effects of smoking cessation with varenicline on antipsychotic drug-induced neurological side effects, we propose a 12 week pilot study of smoking cessation treatment with varenicline in 10 schizophrenia or schizoaffective disorder patients who are actively smoking and have pre-existing TD while receiving stable doses of antipsychotics. Subjects will be followed after a 2 week baseline period to assess changes in smoking status and neurological symptoms using standardized rating scales. The aim is to examine clinically significant effects on antipsychotic-induced neurological side effects that may warrant further investigation.

NCT ID: NCT03494894 Completed - Cystic Fibrosis Clinical Trials

Bacteriological Link Between Upper and Lower Airways in Cystic Fibrosis and Primary Ciliary Dyskinesia

BAVASI
Start date: June 1, 2017
Phase:
Study type: Observational

Cytobacteriological examination of sputum and bacteriological sampling in the middle meatus.

NCT ID: NCT03489785 Recruiting - Clinical trials for Involuntary Movements

Predictive Factors of Unpredicted Movement in Motor Evoked Potential

Start date: June 1, 2003
Phase:
Study type: Observational

The purpose of this study was to identify the predictive factors of unpredicted movement in motor evoked potential (MEP) during intraoperative neurophysiologic monitoring in adult patients undergoing brain surgery.

NCT ID: NCT03370029 Completed - Clinical trials for Primary Ciliary Dyskinesia

Respiratory Muscle Strength, Exercise Capacity and Physical Activity Levels in Children Primary Ciliary Dyskinesia

Start date: October 2016
Phase:
Study type: Observational

Primary ciliary dyskinesia is an autosomal recessive disorder characterized by abnormal ciliary movement and disrupted mucociliary clearance. In uncleaned airways, microorganisms and respiratory irritants cause inflammation and infection. Permanent rhinitis and chronic sputum cough are typical features in primary ciliary dyskinesia patients. Primary ciliary dyskinesia is a disease that threatens lung function from pre-school age. One of the main causes of respiratory muscle weakness in chronic lung diseases diseases is worsening of lung function. Such a weakness causes alveolar hypoventilation, microatelectasis, reduction of the cough strength .The cough strength is important for airway cleaning. Exercise capacity is affected in chronic lung diseases. Assessment of exercise capacity in chronic lung diseases is prognostically important. Reduced exercise capacity and pulmonary function in PCD cause decrease in physical activity level. PCD patients have low quality of life and early recognition has been found to affect the quality of life positively. Children with chronic illness have higher level of depression than healthy children. In literature, no study investigated respiratory muscle strength, exercise capacity and physical activity PCD patients. Therefore, the investigators aimed to compare aforementioned outcomes in PCD patients and healthy controls.

NCT ID: NCT03368170 Completed - Parkinson Disease Clinical Trials

Efficacy and Tolerability of IRL790 in Parkinson's Disease Dyskinesia

Start date: April 12, 2018
Phase: Phase 2
Study type: Interventional

Mesdopetam (IRL790) is an experimental small molecule compound with psychomotor stabilizing properties. The primary target is the dopamine D3 receptor, a target implicated in the generation of levodopa-induced dyskinesia, a side-effect frequently occurring with long-term levodopa treatment in patients with Parkinson's disease. In experimental animals mesdopetam potently reduced levodopa-induced involuntary movement without impairing the antiparkinsonian effect of levodopa. The primary purpose of the trial is to investigate whether mesdopetam given as adjunctive treatment can reduce levodopa induced dyskinesia in patients with Parkinson's disease. The trial will also help to establish the most optimal dosing of the compound.