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Parkinson Disease clinical trials

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NCT ID: NCT03065127 Active, not recruiting - Parkinson Disease Clinical Trials

Investigating Therapies for Freezing of Gait

Start date: February 24, 2017
Phase: N/A
Study type: Interventional

Freezing of gait (FOG) is arguably one of the most debilitating motor symptoms experienced by individuals with Parkinson's disease (PD). FOG may be caused by an overload of cognitive, limbic, and sensorimotor system activity in the basal ganglia. Therefore, the purpose of this study is to evaluate cognitive, limbic, and sensorimotor therapies in individuals with FOG. Participants in this study will undergo all three types of treatments in a randomized counterbalanced order. Each treatment will occur in 1 hour sessions, twice weekly for a period of 4 weeks.

NCT ID: NCT02954978 Active, not recruiting - Parkinson Disease Clinical Trials

Impact of Nilotinib on Safety, Tolerability, Pharmacokinetics and Biomarkers in Parkinson's Disease

PD Nilotinib
Start date: January 2017
Phase: Phase 2
Study type: Interventional

Parkinson's disease (PD) is the second most common neurodegenerative disorder causing motor and non-motor symptoms. PD is characterized by death of dopaminergic (DA) neurons in the substantia nigra (SN) pars compacta and formation of inclusions known as Lewy bodies (LBs) that primarily contain aggregated alpha-Synuclein. Nilotinib (Tasigna®, AMN107, Novartis, Switzerland) is approved by U.S. Food and Drug Administration (FDA) and is well tolerated for CML treatment at oral doses of 600-800mg daily. Nilotinib penetrates the brain and promotes autophagic degradation of alpha-Synuclein and p-Tau, leading to survival of DA neurons and improvement of motor function in PD models. For these studies, Nilotinib (1-10mg/kg daily) was used at significantly less than the clinically approved dose (up to 1200mg daily) in CML.

NCT ID: NCT02937324 Active, not recruiting - Parkinson's Disease Clinical Trials

The CloudUPDRS Smartphone Software in Parkinson's Study.

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

This study compares the validity and usability of smartphone software for home monitoring of symptoms and signs in Parkinson's disease as compared to the current clinical gold standard - the Unified Parkinsons Disease Rating Scale.

NCT ID: NCT02920632 Active, not recruiting - Parkinson Disease Clinical Trials

Cognitive Training in Parkinson Study

cogtips
Start date: September 15, 2017
Phase: N/A
Study type: Interventional

This study evaluates the efficacy of an eight-week online cognitive training program on objective and subjective cognitive functions in Parkinson's disease. Moreover, we intend to map the effect on brain network function, and if cognitive training can prevent the development of PD-MCI/PD-D after one- and two-year follow-up. In this study, two training groups will be compared (N: 70 vs 70). In a part of the participants MRI will be assessed (N: 40 vs. 40). We expect cognitive training to improve cognitive functions, and to improve the efficiency of brain network function. Moreover, we expect that cognitive training can decrease the risk of PD-MCI/PD-D at one- and two-year follow-up.

NCT ID: NCT02914366 Active, not recruiting - Clinical trials for Parkinson's Disease Dementia

Ambroxol as a Treatment for Parkinson's Disease Dementia

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

The present study will test the hypothesis that the medication Ambroxol is safe and well tolerated and will improve cognitive and motor symptoms of Parkinson's Disease Dementia (PDD). Ambroxol has been shown to raise the levels of the enzyme beta-glucocerebrosidase resulting in lower the levels of the protein alpha-synuclein, both of which have been shown to improve cognition in mouse models. This will be a 52 week trial of Ambroxol in 75 individuals with PDD. Participants will undergo clinical, neuropsychological and neuroimaging assessment throughout the study to assess changes.

NCT ID: NCT02906488 Active, not recruiting - Parkinson's Disease Clinical Trials

Special Drug Use-results Survey of Duodopa Enteral Solution in Patients With Parkinson's Disease

Start date: September 12, 2016
Phase:
Study type: Observational

The purpose of this study is to assess the safety and efficacy of long-term use of Duodopa in patients with Parkinkon's disease in actual usage

NCT ID: NCT02881099 Active, not recruiting - Parkinson's Disease Clinical Trials

Parkinson's Repository of Biosamples and Network Datasets (Tracking Parkinson's)

PRoBaND
Start date: February 2012
Phase:
Study type: Observational

Prospective observational study of Parkinson's disease with repeat clinical assessment and biobanking of blood samples.

NCT ID: NCT02864004 Active, not recruiting - Parkinson's Disease Clinical Trials

Apomorphine Pump in Early Stage of Parkinson's Disease (EARLY-PUMP)

EARLY-PUMP
Start date: March 3, 2017
Phase: Phase 3
Study type: Interventional

The aim of the study is to assess the use of the apomorphine pump in earlier stages of Parkinson' Disease (PD), when motor complications have just developed and before patients are significantly affected in their social and occupational functioning. The investigators hypothesize that apomorphine pump is superior in terms of positive impact on quality of life (QoL) to oral medical therapy alone at a relatively early stage of PD, before the appearance of severe disabling motor complications thus favoring the maintain of patients' social and occupational status with a significant positive economic impact of the health system.

NCT ID: NCT02858778 Active, not recruiting - Multiple Sclerosis Clinical Trials

Timing of Acute Palliative Care Consultation in Critically Ill Patients

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

A prospective randomized controlled trial studying the ordering of palliative care consultations in the emergency department (Ig) versus later palliative care consultations in the hospital--ICU or hospital ward(Cg). Patients will be randomly allocated to Ig or Cg with a 1:1 ratio.

NCT ID: NCT02827812 Active, not recruiting - Parkinson's Disease Clinical Trials

Telemedicine Program in Parkinson's Disease (TELEPARK)

TELEPARK
Start date: June 2016
Phase: N/A
Study type: Interventional

Parkinson's disease (PD) is a chronic neurodegenerative disease due to the loss of dopaminergic neurons in the substantia nigra, leading to motor symptoms of tremor, rigidity, and bradykinesia, as well as an array of non-motor symptoms that affect cognition, sleep, behaviour, and the autonomic nervous system. Lifelong rehabilitation measures, along with medication treatment, are the major components of patient management. Physical exercises positively affect patients' quality of life (QOL) and their functional capacities. Poor adherence to rehabilitation, limited patient education, and access to specialized care can be barriers to treatment. A number of papers in fact report that telemedicine is an acceptable means of care delivery reduces travel burdens and may improve patient outcomes. However, most of these studies were not randomized or controlled and did not include nursing home patients, who may benefit the most from specialty care. Moreover, there is no evidence supporting the use of telerehabilitation for physical assessments of people with PD. For this reason investigators hypothesize that a home telerehabilitation system guiding patients in following their exercise program combined with a computerized decision-support tool monitoring patient performance, would be feasible for and acceptable to patients with PD and would improve functional status.