Effects of Rasagiline on Sleep Disturbances in Parkinson's Disease

Sleep Disturbances Clinical Trial

— RaSPar  

Official title:

Effects of Rasagiline on Sleep Disturbances in PD: A Single Center, Randomized, Double-blind, Placebo run-in, Polysomnographic Clinical Phase IV Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01442610
• Other study ID #: TUD-RaSPar-051
• Status: Completed
• Phase: Phase 4
• First received: September 23, 2011
• Last updated: January 20, 2016
• Start date: October 2011
• Est. completion date: September 2015

Study information

• Verified date: January 2016
• Source: Technische Universität Dresden
• Contact: n/a
• Is FDA regulated: No
• Health authority: Germany: Federal Institute for Drugs and Medical Devices
• Study type: Interventional

Clinical Trial Summary

As the MAO-B inhibitor rasagiline is able to improve motor skills it might have positive effects on sleep disruption by reducing nocturnal akinesia. As it was reported to cause only minor sleep disruption in PD Patients, it might be able to improve sleep architecture. The investigators thus study the effects of Rasagiline on sleep disturbances measured by polysomnographic (PSG) evaluation of sleep efficacy and PDSS-2. Secondary measures are other sleep variables measured by PSG, sleep quality and daytime sleepiness assessed by standardized scales as well as cognitive function, depression and QoL index.

Description:

Sleeping disorders are very common in patients with Parkinson's Disease (PD). Mainly initiation and maintenance of sleep is disturbed, therefore many patients suffer from daytime sleepiness and sleep attacks. Polysomnographic studies showed increased sleep fragmentation and frequent awakenings, increased amount of wakefulness during time in bed as well as reduced sleep efficacy and deep sleep time. In addition, increased sleep latency, REM-latency and decreased amounts of REM sleep were documented.

PD patients also suffer from primary sleep disorders like sleep disordered breathing and especially REM sleep behaviour disorder (RBD)and periodic limb movements in sleep (PLMS).

Not only neurochemical changes affecting cholinergic and monoaminergic systems, nocturnal hypokinesia and rigidity and painful dystonia due to the disease itself, but also medication side effects lead to impaired sleep-wake-control and reduced REM sleep.

Although levodopa medication and dopamine agonists reduce nocturnal hypokinesia and therefore improve insomnia they also have a potential impact on daytime sleepiness and are able to cause sleep disruption. The impact of dopaminergic therapy is complex showing biphasic effects with increased wakefulness and decreased REM-sleep frequency via stimulation of dopamine D1 receptors whereas low doses promote sleep via dopamine D2 receptors. In addition, acting of dopamine agonists via dopamine D3 receptors might be responsible for daytime sleepiness and sleep attacks.

However, as stimulation of the subthalamic nucleus improves mainly motor skills but also shows an important increase in sleep duration and quality, it could be suggested that by decreasing nocturnal hypokinesia improvement in sleep quality can be achieved.

Rasagiline mesylate was developed as a selective and irreversible MAO-B- inhibitor which is

• unlike Selegiline - not metabolized to amphetamine derivates which are found to be partly responsible for negative effects on RBD and REM-sleep as well as sleep efficacy. Rasagiline is able to delay the need for initiating dopaminergic therapy, improves motor function in early and moderate to advanced PD and was shown to exhibit neuroprotective potential.

As different mechanisms of dopaminergic medication on different dopamine receptors are still not fully elucidated and in contrast to selegiline no side effects due to development of amphetamine derivates need to be taken into consideration, this study is to aim at evaluating the effects on sleep and daytime sleepiness of treatment with Rasagiline mesylate.

As Rasagiline is able to improve motor skills it might have positive effects on sleep disruption by reducing nocturnal akinesia. As it was reported to cause less sleep disruption in PD Patients than placebo it might be able to improve sleep architecture. Until now no clinical trial using polysomnographic techniques was performed to evaluate the effects of Rasagiline on sleep.

To study the effects of Rasagiline on sleep disturbances measured by polysomnographic (PSG) evaluation of sleep efficacy and PDSS-2.

Secondary measures are other sleep variables measured by PSG. In addition, sleep quality and daytime sleepiness assessed by standardized scales as well as cognitive function, depression indices and QoL index are measured.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: September 2015
• Est. primary completion date: March 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 50 Years to 85 Years

Eligibility

Inclusion Criteria:

• Male or female outpatients

• Age from 50 to 85 years

• Definite Parkinson's disease according to UK brain bank criteria

• Hoehn & Yahr I-III

• Relevant sleep disturbance (> 5 point in PSQI)

• Patient must be able to complete questionaires

• Stable antiparkinsonian medication for at least 4 weeks prior to screening

• Antiparkinsonian medication should be stable 30 days prior to screening until 10 days after end of study

• Written informed consent

Exclusion Criteria:

• Overreaction/allergies to study drug or one of its components

• Pregnancy and/or lactation period

• Women with childbearing potential not practicing an acceptable method of contraception (Pearl-Index <1)

• Non-permitted medication within two weeks prior to study inclusion and during study:

Hypnotics, Amantadine, MAO inhibitors, SSRIs, SNRIs, tricyclic and tetracyclic antidepressants, all neuroleptics except clozapine and quetiapine

• Non-permitted medication during study: CYP P450 1A2 inhibitors (a.e. Ciprofloxacin, Cimetidine, Clarithromycin, Erythromycin, systemic Estrogen, Fluvoxamine, Isoniazid, Ketoconazole, Levofloxacin, Norfloxacin, Mexiletine, Paroxetine, Propafenone, Zileuton, Disulfiram, Ginseng, grapefruit juice, Ephedrine).

• Planned participation or participation in another clinical trial during the last 4 weeks prior to screening and during the whole trial period

• Epilepsy or epileptic seizure in the history

• Significant renal or hepatic impairment

• Legal incapacity or limited legal capacity

• Dementia or other psychiatric illness that prevent from giving informed consent.

• Any clinically significant medical illnesses which interfere with capability to participate in study

• History of sleep related breathing disorder or severe OSAS as characterized by PSG (> 30 AHI)

• Severe Depression (BDI > 17)

• Known history of cardiac arrhythmias, angina pectoris, narrow angle glaucoma, residual urine caused by benign prostatic hyperplasia, pheochromocytoma

• Patients requiring elective surgery requiring general anaesthesia during study period

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Dyssomnias
• Parasomnias
• Parkinson Disease
• Parkinsons's Disease
• Sleep Disorders
• Sleep Disturbances

Intervention

Drug:
• Rasagiline
Rasagiline tablets 1mg once daily for 8 weeks
• Placebo
Placebo 1tablet once daily for 8 weeks

Locations

Country	Name	City	State
Germany	Dresden University of Technology, Dept. of Neurology	Dresden

Sponsors (2)

Lead Sponsor	Collaborator
Technische Universität Dresden	Teva Pharmaceutical Industries

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in sleep efficacy	Change from baseline in sleep efficacy (% in time in bed (TIB) / sleep partial time (SPT)) in polysomnography at 8 weeks	baseline and 8 weeks	No
Primary	Change in PDSS-2	Change from baseline in sleep quality at 8 weeks	Baseline and 8 weeks	No
Secondary	Change in other sleep parameters	Change from baseline in sleep parameters e.g. portion of REM-sleep (%), portion of slow wave sleep (%), portion of light sleep (%), sleep latency (min), REM-sleep latency (min) in polysomnography at 8 weeks	baseline and 8 weeks	No
Secondary	Electrocardiography	Number of participants with adverse events	baseline and 8 weeks	Yes
Secondary	Laboratory parameter	Number of participants with adverse events	baseline and 8 weeks	Yes