Ramelteon (ROZEREM) in the Treatment of Sleep Disturbances Associated With Parkinson's Disease

Condition(s) targeted: Parkinson's Disease

Intervention: ROZEREM (Drug); Ramelteon (Drug)

Phase: Phase 4

Status: Recruiting

Sponsored by: Southern California Institute for Research and Education

Official(s) and/or principal investigator(s):
Clifford Widmark, M.D., Principal Investigator, Affiliation: VA Long Beach Healthcare System

Patients with Parkinson's disease represent a significant proportion of VA elderly patients. Sleep disturbances and caregiver burnout association with this condition represent a significant problem. In this study, the investigators propose to perform an evaluation of a fixed doe of ramelteon on sleep in VA outpatients diagnosed with Parkinson's disease.

The hypothesis to be examined is that ramelteon will improve the quality of sleep in patients with Parkinson's disease while indirectly improving the quality of life for the patients and caregivers. The investigators further hypothesize that these changes will occur through restructuring and normalization of the sleep architecture.

Official title: Ramelteon (ROZEREM) in the Treatment of Sleep Disturbances Associated With Parkinson's Disease

Study design: Treatment, Randomized, Double Blind (Subject, Caregiver), Placebo Control, Crossover Assignment, Efficacy Study

Primary outcome:

Neuropsychiatric Inventory with Caregiver Distress (NPI-D) Sleep Behavior Subscale

The Epworth Sleepiness Scale

Sleep Disorders Questionnaire (short form)

Secondary outcome:

Memory - Hopkins Verbal Learning Test (HVLT)

Movement - Abnormal Involuntary Movement Scale (AIMS)

Movement - Unified Parkinson's Disease Rating Scale (UPDRS)

Movement - Continuous motor activity (actigraphy/motion logger)

Detailed description: It is well established that sleep disturbances are common in patients with neurodegenerative disorders such as Parkinson's disease. Together with psychosis and other behavioral abnormalities they contribute to the stress, anxiety and cognitive decline of patients, caregiver burnout and depression, as well as health care provider frustration. The mechanisms of the sleep disturbances in these conditions are still poorly understood and no rational or effective treatments have been proposed. Recent data from a study of ramelteon in the elderly showed a striking ability of this compound to improve quality of sleep disturbances in Parkinson's disease.

Objectives of this study are:

- To examine the effects of ramelteon on the quality of sleep using sleep evaluation

instruments (SDQ-Sleep Disorder Questionnaire and Neuropsychiatric Inventory with Caregiver Distress (NPI-D) Sleep Behavior Subscale administered to the patient and/or their bed partner.

- To examine the effects of ramelteon on daytime sleepiness and memory using Epworth

Sleepiness Scale (ESS) and Hopkins Verbal Learning Test (HVLT).

- To examine the effects of ramelteon on the sleep/wake cycle and day/night activity

patterns over a prolonged period of time (1 week) using a motion logger (continuous motor activity recording device) and computerized data analysis.

- To examine the effects of ramelteon on sleep architecture in a sample of patients with

confirmed sleep disturbance, before and after ramelteon treatment by using polysomnography.

Minimum age: 45 Years. Maximum age: 85 Years. Gender(s): Both.

Criteria:

Inclusion Criteria:

- 45-85 years of age and living in the community

- Male or female of non-child bearing potentials (non-child bearing is defined as at

lease 6 months post-menopause or surgically sterile)

- Must have a diagnosis of Parkinson's disease

- Must have complaints of sleep disturbance

Exclusion Criteria:

- Patients with diagnosis of or those meeting DSM-IV criteria for major depression,

schizophrenia or schizoaffective disorder, bipolar disorder, substance abuse disorder, other mental illness that is known to contribute to sleep disturbance, epilepsy, other medical conditions that are known to cause or contribute to sleep disturbances

- Patients currently using melatonin or ramelteon, hypnotics, benzodiazepines,

antidepressants, blood-brain barrier permeable beta blockers, steroids, antipsychotics

- Patients with clinically significant blood or urine abnormalities

- Patients who have taken any investigational drug less than 1 month prior to the

baseline visit

- Patients with multiple concomitant disorders with or without medications thought to

produce sleep disturbances

- Patients with pre-existing sleep disturbances unrelated to Parkinson's disease

- Patients with severe hepatic impairment (Child-Pugh Class C)

- Patients with severe COPD (those with elevated pCO2 levels or those needing nocturnal

oxygen therapy

- Patients with severe sleep apnea

- Patients who have sensitivity to ramelteon or any constituents of the Rozerem

preparation

- Patients taking rifampin or potent inducers of CYP1A2, CYP3A4, CYP2C9 (ketoconazole,

fluconazole)

- Patients living in a nursing home. Those living in assisted living facilities and

board and care facilities may be included

- Patients unable to comply with the study protocol

VA Long Beach Healthcare System, Long Beach, California 90822, United States; Recruiting
Jennifer Koontz, M.A, Phone: 562-826-8000, Ext: 4313, Email: Jennifer.Koontz@va.gov
Gardner Ricca, Phone: 562-826-8000, Ext: 4313, Email: Ricca.Gardner@va.gov
Clifford Widmark, M.D., Principal Investigator

Southern California Institute for Research and Education website

Starting date: June 2007
Ending date: February 2009
Last updated: December 23, 2008