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Parkinson Disease clinical trials

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NCT ID: NCT02039024 Completed - Parkinson's Disease Clinical Trials

Imaging Non-motor Symptoms of Parkinson's Disease by Novel 18F-DTBZ and Florbetapir F-18 PET

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

The primary objective of this protocol is to investigate the monoaminergic (dopamine、serotonin、and norepinephrine ) nervous system and amyloid deposition in Parkinson's disease patients with non-motor symptoms (focus on impulse control disorders and dementia) by novel 18F-DTBZ and Florbetapir F-18 PET imaging. This study will compare the amyloid deposition of brain by florbetapir F-18 PET imaging and monoaminergic function by18F- DTBZ PET in NC group, PD group, PDD group, AD group. Investigators will also analyze monoaminergic function by18F- DTBZ PET in PDI group.

NCT ID: NCT02038608 Completed - Parkinson's Disease Clinical Trials

Compensatory Mechanisms in Parkinson Disease (PD)

CompensationPD
Start date: December 2014
Phase: N/A
Study type: Interventional

Parkinson's disease is characterized by a large number of non motor, especially neuropsychiatric, signs. Their pathophysiology is complex but the role of dopaminergic and serotoninergic systems dysfunction is suggested by several studies. In addition, the serotoninergic system is involved in the pathophysiology of dyskinesias. Very few studies have analyzed the abnormalities of these two neurotransmission systems at disease onset, in de novo PD patients. Furthermore, the parallel evolution of the degeneration of the dopaminergic and serotoninergic systems with disease progression remains unknown. Thus the present study aims at determining, by using PET and 11C-PE2I and 11C-DASB the respective role of the serotoninergic and dopaminergic systems dysfunction in motor and non motor manifestations in PD, at different evolution stages.

NCT ID: NCT02034357 Completed - Parkinson's Disease Clinical Trials

Sleep Disordered Breathing and Its Impact on Neuro-cognitive Performance and Quality of Life in Parkinson Disease

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

The purpose of this study is to determine the impact of sleep and breathing problems during sleep on memory, attention, and general well being (quality of life) in people with Parkinson Disease.

NCT ID: NCT02034318 Completed - Parkinson's Disease Clinical Trials

Fatigue and Cardiac Sympathetic Denervation in Parkinson Disease

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

The purpose of this research study is to learn about a possible association between cardiac denervation (the breaking down of nerves in the heart) and the development of fatigue in Parkinson's disease (PD).

NCT ID: NCT02028858 Completed - Parkinson's Disease Clinical Trials

Cannabis and Parkinson's Disease Tremor: A Natural History Study

Start date: November 2013
Phase: N/A
Study type: Observational

This is a prospective, observational study designed to describe the effects of Cannabis on Parkinson's Disease tremor.

NCT ID: NCT02025517 Completed - Parkinson's Disease Clinical Trials

Gait Training With Cognitive Tasks in Parkinson's Disease

Start date: August 2012
Phase: N/A
Study type: Interventional

Treadmill gait training combined with cognitive tasks in Parkinson's disease.

NCT ID: NCT02023034 Completed - Parkinson Disease Clinical Trials

Virtual Exercises in Patients With Parkinson's Disease.

Start date: February 2013
Phase: N/A
Study type: Interventional

Introduction: Although the motor changes are well determined in Parkinson's disease (PD), few studies describe the effects the virtual exercises on the clinical and functional outcomes in this disease. Objectives: To analyze the effectiveness of virtual exercises on functional exercise capacity, fatigue and quality of life in patients with PD. Methods: 20 subjects, 60 years old will be included, who will be randomized into 2 groups: group of virtual exercises associated with conventional exercises (n = 10) and control group with conventional exercise group (n = 10). The following variables are evaluated: functional exercise through walking test in 6 minutes, fatigue by the Fatigue Severity Scale and Quality of Life through Quality of Life Questionnaire-PDQ-39.

NCT ID: NCT02021903 Completed - Clinical trials for Parkinsonian Disorders

Post-prandial Hypotension and Sleepiness in Parkinson's Disease and Other Synucleinopathies

HYPOSOMNPARK
Start date: May 2012
Phase: N/A
Study type: Interventional

Excessive daytime sleepiness (EDS) is observed in 30 to 50 % of patients with Parkinson's disease (PD) patients, Dementia with Lewy Bodies (DLB) and Multiple System Atrophy (MSA). It is a major complain and represents a socially relevant problem as unintended episodes of sleep can also occur while driving for example. Arterial hypotension is frequently observed in patients with PD, DLB and MSA and considered as a marker of autonomic failure. Sleepiness is known to occur preferentially when patients are having arterial hypotension whatever the cause (i.e. postprandial period, administration of hypotensive medication such as dopamine agonists). We hypothesize that arterial hypotension is associated with abnormal sleepiness. We have observed this association in an on-going epidemiological survey Hyperglycaemia induced by oral glucose load - a standardized model simulating food intake during a meal - provokes arterial hypotension in the majority of Parkinson's disease patients with dysautonomia. It can be hypothesised that sleep attacks in these patients could be mediated by this fall in blood pressure.

NCT ID: NCT02017938 Completed - Clinical trials for Parkinson's Disease (PD)

Establishing the Central and Peripheral Fatigue Indexes and VR Based Anti-fatigue Training Paradigm for Individuals With Parkinson Disease

Start date: December 10, 2014
Phase: N/A
Study type: Interventional

Fatigue is one of the most common symptoms in individuals with Parkinson's Disease (PD). Past researches indicated that more than half of the individuals with PD demonstrated fatigue symptom. The severity of fatigue was also correlated to the quality of life in individuals with PD. Finding the contributions of the central and the peripheral factors to fatigue, building reliable fatigue indexes, and developing an effective training program for individuals with PD are very important. The purpose of this project is to develop non-invasive method to monitor central and peripheral fatigue, to establish Virtual Reality(VR) anti-fatigue ergo cycling training paradigm, and to evaluate the long term training effect in individuals with PD.

NCT ID: NCT02015806 Completed - Breast Cancer Clinical Trials

Robust Evaluation to Measure Improvements in Nonadherence From Low-cost Devices

REMIND
Start date: March 2014
Phase: N/A
Study type: Interventional

The aim of this study is to determine whether adherence to oral maintenance medications differs for patients randomized to receive a RxTimerCap, a Take-N-Slide, a standard pillbox, or none of these devices, with the hypothesis that low-touch devices improve adherence over control and that the increase in adherence is agnostic across devices.