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Dyskinesias clinical trials

View clinical trials related to Dyskinesias.

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NCT ID: NCT02840760 Recruiting - Tardive Dyskinesia Clinical Trials

Repetitive Transcranial Magnetic Stimulation for the Treatment of the Tardive Dyskinesia.

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

The purpose of this study is to explore the therapeutic effect and mechanism of transcranial magnetic stimulation (rTMS) in the treatment of the tardive dyskinesia.

NCT ID: NCT02578849 Recruiting - Parkinson´s Disease Clinical Trials

Common Noradrenergic Mechanisms in Parkinson´s Disease and L-DOPA Induced Dyskinesia

NORAPARK
Start date: January 2012
Phase: N/A
Study type: Observational

The aims of this proposal include tests of hypotheses of the pathogenetic mechanisms of noradrenergic neurotransmission in Parkinson's disease in vivo, using positron emission tomography of patients with early and advanced Parkinson's disease with or without 3,4 L-dihydroxyphenylalanine (L-DOPA) - induced dyskinesia or co-morbid depression, and evaluation of whether these mechanisms can be influenced therapeutically. Hypotheses: 1. The investigators argue that release in human cortical and subcortical brain regions of norepinephrine (NE) derived from metabolism of exogenousL-DOPA is greater in Parkinson's disease patients with L-DOPA- induced dyskinesia than in patients without this complication. This hypothesis will be tested by measuring antagonist [11C]yohimbine binding to alpha-2 adrenoceptors before and after L-DOPA challenge. 2. If so, it is argued that the greater rise of norepinephrine, measured as [11C]yohimbine displacement after L-DOPA challenge, is the result of down-regulation or loss of norepinephrine transporters. This hypothesis will be tested by measuring the binding of [11C]MeNER, a tracer of norepinephrine transporters. 3. If so, the investigators argue that the greater decline of [11C]MeNER binding is significantly correlated to the symptoms of Parkinson's disease, as proof that patients with more severe loss of noradrenergic terminals exhibit more severe motor deficits.

NCT ID: NCT02439125 Recruiting - Parkinson's Disease Clinical Trials

A Study to Examine the Efficacy and Safety of Eltoprazine HCl for Treatment of Levodopa-induced Dyskinesia in Parkinson's Disease Patients

Start date: May 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety, tolerability and efficacy of eltoprazine to treat levodopa-induced dyskinesia in patients with Parkinson's disease

NCT ID: NCT02419365 Recruiting - Clinical trials for Primary Ciliary Dyskinesia (PCD)

International Primary Ciliary Dyskinesia (PCD) Registry

PCDregistry
Start date: January 2014
Phase:
Study type: Observational [Patient Registry]

The purpose of the international prospective PCD Patient Registry is to systematically measure, survey and compare different aspects of PCD manifestation, course and treatment, to provide data for epidemiological research and to identify special patient groups suitable for multi-center trials. This International PCD Registry is also part of the European Reference Network ERN-LUNG. We follow the recommendations of the EU Expert Committee on Rare Diseases (EUCERD), which recommend an international interoperability of registries and databases to pool and exchange knowledge and data on rare diseases.

NCT ID: NCT02195115 Recruiting - Clinical trials for Gallbladder Dyskinesia

Trial of Laparoscopic Cholecystectomy vs. Non-operative Treatment for Gallbladder Dyskinesia

Start date: February 2014
Phase: Phase 2
Study type: Interventional

The goal of this study is to challenge the existing clinical practice of employing laparoscopic cholecystectomy as the treatment for gallbladder dyskinesia by comparing it to a regimen of active non-surgical therapy.

NCT ID: NCT01929356 Recruiting - Clinical trials for Primary Ciliary Dyskinesia

Chest Physiotherapy and Lung Function in Primary Ciliary Dyskinesia

Start date: June 30, 2020
Phase: N/A
Study type: Interventional

Primary ciliary dyskinesia (PCD) is a rare disease, caused by impairment of the motile cilia. Patients present with chronic upper and lower respiratory tract infections. The therapy is mainly supportive and based on that of cystic fibrosis. Chest physiotherapy is one of the cornerstones of the therapy, however the influence of chest physiotherapy on lung function (short term and long term) is not clear. For interpretation of longitudinal lung function data it is important to examine the short time effect of chest physiotherapy. We hypothesize that a session of chest physiotherapy improves lung function and that thus lung function tests must be performed in a standardized way.

NCT ID: NCT01338662 Recruiting - Parkinson`s Disease Clinical Trials

Comparison of the Incidence of Dyskinesia in Parkinson`s Disease Who Were Treated With Amantadine or Dopamine Agonist

Start date: May 2011
Phase: N/A
Study type: Observational

The purpose of this study is to compare the onset time and severity of dyskinesia in amantadine or Dopamine agonist initial treated groups in Parkinson`s disease.

NCT ID: NCT01246258 Recruiting - Clinical trials for Primary Ciliary Dyskinesia

Otolith Function in Patients With Primary Ciliary Dyskinesia

Start date: September 2010
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether patients with primary ciliary dyskinesia (PCD) have reduced or absent otolith function.The otolith system is a specific part of the inner ear vestibular (balance) system that detects linear movement.

NCT ID: NCT01070914 Recruiting - Clinical trials for Primary Ciliary Dyskinesia

Early Detection and Characterization of Primary Ciliary Dyskinesia

Start date: June 2011
Phase: N/A
Study type: Observational

Primary Ciliary Dyskinesia (PCD) is a severe genetic disorder caused by various mutations in genes affecting ciliary motility. Various new and complementary diagnostic techniques, including measurements of nasal nitric oxide (NO), Video Microscopy (VM), Immunoflourescence (IF) and genetic analysis have recently been recognized as simpler and more accurate modalities for the diagnosis and characterization of patients with PCD compared to electron microscopy. While considered a rare disease worldwide, PCD is more prevalent among highly consanguineous populations, such as those found in Israel. We hypothesize that using modern state of the art and novel test modalities on a national scale in Israel will improve diagnosis, improve phenotypic-genotypic correlations and create a national registry for PCD.

NCT ID: NCT00837707 Recruiting - Clinical trials for Dyskinesia, Drug-Induced

Aripiprazole for Neuroleptic-Induced Tardive Dyskinesia

Start date: June 2008
Phase: Phase 4
Study type: Interventional

The aim of the present study was to investigate the efficacy of aripiprazole in management of pre-existing neuroleptic-induced tardive dyskinesia