Parkinson Disease Clinical Trial
Official title:
Uncontrolled Pilot Trial of Transnasal Nicotine in Parkinson Disease
The widely observed inverse relationship between smoking and Parkinson's Disease (PD) and the results of numerous preclinical studies indicating neuroprotective effects of nicotine, suggest a possible novel intervention in PD. In our opinion, an optimal nicotinic therapy in PD would consist of pulsatile nicotine delivery (e.g. via nasal spray) similar to pulsatile nicotine obtained via smoking. The investigators believe that pulsatile stimulation of the central nicotinic receptors (achievable via nasal spray) would affect the dynamic of the nicotinic receptors much more desirably and similar to smoking compared to continuous nicotine administration via patch, which might result in continuous nicotinic receptor desensitization. Thus, this pilot trial seeks to evaluate the efficacy of nicotine nasal spray (Nicotrol NS®) in symptomatology of PD. For this purpose, a total of 6 non-smoking patients at intermediate disease stages (2-3 of Hoehn and Yahr scale) and receiving conventional therapy for PD will be recruited at the "Instituto Nacional de Neurología y Neurocirugía, (Manuel Velasco Suárez)" in Mexico City. Nicotrol NS® in incremental dosing (up to 10 mg/day) regimens will be added to the current medications to each patient during the first week. This will be maintained for up to 1 month. Motor and non-motor aspects of PD will be evaluated. The investigators expect significant improvement of motor and non-motor symptoms in all patients receiving Nicotrol NS® during therapy and a reversal during withdrawal.
Parkinson's disease (PD), the second most common progressive neurodegenerative disorder, is
associated with loss of dopaminergic neurons in the substantia nigra pars compacta that leads
to striatal dopamine deficiency. This dopaminergic loss results in motor deficits
characterized by: akinesia, rigidity, resting tremor and postural instability as well as
non-motor symptoms that might also involve other neurotransmitter systems. The non-motor
symptoms may include: cognitive deficits (e.g., mild to severe memory impairment), emotional
changes (e.g., depression, apathy and anxiety), sleep perturbations (e.g.,
insomnia/hypersomnia), autonomic dysfunction (e.g., bladder disturbances, orthostatic
hypotension, sweating), sensory symptoms (e.g., pain, visual and olfactory deficits) and
gastrointestinal symptoms (e.g., constipation, nausea).
Parkinson's disease current treatment of choice is replacement of dopamine with its precursor
Levodopa (L-Dopa), which unfortunately loses its effectiveness and can cause dyskinesia
following prolonged usage. This fact motivates the search for new pharmacological strategies
to better control the symptoms and/or progression of the disease.
The inverse relationship between smoking and PD has been confirmed by a number of
epidemiological studies. Moreover, numerous preclinical studies indicate neuroprotective
effects of nicotine. Thus, nicotine may offer a novel intervention in PD. Although use of
nicotine patch has been suggested in some neurodegenerative disorders, including PD, the
investigators believe that the key for success with nicotinic intervention, particularly in
PD, relies on mode of nicotine administration. In our opinion, an optimal nicotinic therapy
in PD would consist of pulsatile nicotine delivery (e.g. via nasal spray) similar to
pulsatile nicotine obtained via smoking. Pulsatile stimulation of the central nicotinic
receptors (achievable via nasal spray) would affect the dynamic of the nicotinic receptors
much more desirably than continuous nicotine administration via patch, which can result in
continuous nicotinic receptor desensitization. The investigators also believe that nicotine
delivered via nasal spray, in addition to its potential usefulness for improving motor
dysfunctions, may also be helpful in non-motor symptoms (e.g. cognitive decline and
depression) that are commonly associated with neurological disorders such as PD.
Thus, this pilot clinical trial seeks to evaluate the efficacy of treatment during one month
with nicotine nasal spray (Nicotrol NS®) in motor and non-motor aspects of PD.
Hypothesis: Scores of the Movement Disorders Society Unified Parkinson Disease Rating Scale
(MDS-UPDRS) for motor and non-motor symptomatology will decrease after 1 month of treatment
with nicotine nasal spray (Nicotrol) in patients with PD (stages 2-3 of Hoehn & Yahr).
Research question: Can controlled doses of nicotine administered via nasal spray decrease the
severity of PD (stages 2-3 of Hoehn & Yahr) using MDS-UPDRS scores?
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