Study of the Efficacy of N-acetylcysteine (NAC) on Impulse Control Disorders (NoISE-PD)

Centre Hospitalier Universitaire, Amiens

Status and phase: Unknown; Phase 3

Conditions: Impulse Control Disorder; Parkinson

Treatments: Biological: Variation of behaviors of Parkinson's disease

Study type: Interventional

Funder types: Other

Identifiers

NCT03146130

PI2016_843_0002

Details and patient eligibility

About

Impulse control disorders encountered in Parkinson's disease (PD) are induced by dopaminergic medications and their frequency is estimated to be nearly 20%, mainly under dopaminergic agonists (AD).

Full description

Impulse control disorders encountered in Parkinson's disease (PD) are induced by dopaminergic medications and their frequency is estimated to be nearly 20%, mainly under dopaminergic agonists (AD). They constitute a major public health issue due to their sometimes dramatic socio-occupational and judicial consequences. Most often the therapeutic strategy is to reduce or even stop AD, which can lead to withdrawal symptoms, apathy or aggravation of motor signs.

N-acetylcysteine (NAC) may have an interest in the treatment of ICD. This molecule reduces "craving" in addictions by substance abuse, but also in behavioral addictions, with as a potential mechanism a reduction in levels of plasma alphasynuclein.

The main objective of this randomized, double-blind, placebo-controlled, multicenter controlled trial is to demonstrate that a 10-week NAC add-on treatment, compared to placebo, improves the behavioral addictions of Moderate in the MP. The main endpoint will be the variation of the subdivision of the hyperdopaminergic behaviors of the Ardouin Parkinson's Disease Behavioral Assessment (ECMP) scale between the baseline and after 10 weeks of treatment.

Enrollment: 70 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Parkinson's disease according to UKPDSBB criteria
• Subject aged 18 to 80
• Presence of a mild to moderate impulse control disorder defined by an ECD hyperdopaminergic sub-score (part IV) between 3 and 22 associated with the investigator's assessment
• MMSE ≥ 24
• Ongoing treatment with dopaminergic agonist and / or levodopa
• No change in antiparkinsonian and / or psychotropic treatment in the month preceding inclusion
• Expected stability of antiparkinsonian and / or psychotropic treatment during the study period
• Informed patient consent
• Patient supported by social security
• Presence of a caregiver

Exclusion criteria

• Severe TCI defined by a hyperdopaminergic sub-score at ECMP (part IV) greater than 23 associated with the investigator's assessment
• Patient with TCI suspected of having serious legal and / or relationship problems during the study period
• Adaptation of the anti-parkinsonian and / or psychotropic treatment (cf section 6.2) probably necessary during the duration of the study
• Patient treated with naltrexone, amantadine, antipsychotic in the 6 weeks prior to inclusion
• Patient under tutorship or curatorship
• History of hypersensitivity to any of the components or to any of the excipients
• Fructose intolerance, glucose-galactose malabsorption syndrome or sucrase / isomaltase deficiency
• Gastrointestinal duodenal ulcer in progress
• Pregnancy, breastfeeding
• Patients with contra-indicated treatments in association with NAC
• Patient with phenylketonuria
• Patients with proven difficulty in expectorating
• Patients with an asthmatic risk that can lead to bronchospasm
• Patients with intolerance to histamine

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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70 participants in 2 patient groups, including a placebo group

Patient treated with N-acetylcysteine

Active Comparator group

Description:

Patients randomise in the drug group

Treatment:

Biological: Variation of behaviors of Parkinson's disease

Patient treated with placebo

Placebo Comparator group

Description:

Patients randomise in the placebo group

Treatment:

Biological: Variation of behaviors of Parkinson's disease