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Dyskinesias clinical trials

View clinical trials related to Dyskinesias.

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NCT ID: NCT03704207 Recruiting - Clinical trials for Primary Ciliary Dyskinesia

Utility of PCD Diagnostics to Improve Clinical Care

Start date: June 1, 2017
Phase: N/A
Study type: Interventional

This is a study evaluating the utility of current Primary Ciliary Dyskinesia (PCD) diagnostic tests, including nasal nitric oxide testing.

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: 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: 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: 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: NCT03320382 Recruiting - Asthma Clinical Trials

Multiple Breath Washout, a Clinimetric Dataset

Start date: May 5, 2017
Phase:
Study type: Observational

Monitoring patients with chronic, inflammatory airways disease particularly in the early stages is hampered by the relative insensitivity of current outcome measures to detect subtle changes. Multiple breath washout is a potential sensitive test that is a useful readout of disease at these early stages but it lacks standardisation and knowledge of variability with reference to standard lung function measures. This is a Cross sectional and longitudinal observation study. The hypothesis is that multiple breath washout-derived indices will provide a robust signal of gas mixing inhomogeneity, correlating with conventional measures of airway disease severity. Multiple breath washout performed on different devices will generate indices which correlate but differ in value.

NCT ID: NCT03279965 Recruiting - Cystic Fibrosis Clinical Trials

MRI in Cystic Fibrosis and Primary Ciliary Dyskinesia

Start date: May 5, 2017
Phase: N/A
Study type: Observational

This is a small pilot / feasibility study (Approximately 50 patients) to assess the possibility of clinical implementation of MRI assessment of patients with cystic fibrosis and primary ciliary dyskinesia. Patients will undergo their standard CT imaging and lung function investigations and additionally will undergo MRI examination. Reports from CT (the current gold standard) and MRI will be assessed for concordance and patient acceptability and examination implementation costs will also be assessed. Novel MRI-based potential markers of CF and PCD disease state will also be assessed.

NCT ID: NCT03256773 Recruiting - Covid19 Clinical Trials

High Resolution Micro OCT Imaging

Start date: April 15, 2016
Phase:
Study type: Observational

The purpose of this study is to learn about using the imaging to make images of the lungs and nose with the long-term goal of the research leading to potential treatments and new therapies for patients with cystic fibrosis.

NCT ID: NCT03062033 Recruiting - Tardive Dyskinesia Clinical Trials

Real‐World Evaluation Screening Study and Registry of Dyskinesia in Patients Taking Antipsychotic Agents

RE-Kinect
Start date: April 4, 2017
Phase: N/A
Study type: Observational [Patient Registry]

Prospective study to quantify the prevalence of possible tardive dyskinesia (TD) in outpatient psychiatry practices in the United States (US), as well as to describe the associated disease burden in a cohort of patients with one or more psychiatric disorders and a cumulative lifetime exposure to antipsychotic medication of three months or more.