REM Sleep Behavior Disorder Clinical Trial
Official title:
Effect of Clonazepam on REM Sleep Behavior Disorder in Patients With Parkinsonism: a Prospective, Randomized, Double-blind and Placebo-controlled Trial
The purpose of this study is to determine whether clonazepam is effective and safe in the treatment of rapid eye movement behavior disorder (RBD) of patients with Parkinson's disease (PD).
Status | Completed |
Enrollment | 40 |
Est. completion date | March 2016 |
Est. primary completion date | March 2016 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 30 Years and older |
Eligibility |
Inclusion Criteria: - Subject was enrolled voluntarily and understood the contents of this clinical trial - Subject was diagnosed as Parkinson disease (PD) or Parkinson's syndrome - Hoehn and Yahr (H&Y) stage 1, 2, or 3 - Existence of caregivers who can provide a information about symptoms of rapid eye movement sleep disorder (RBD) of the participant - Existence of RBD by answering "yes" to the question (RBD-1Q): "Have you ever been told, or suspected yourself, that you seem to 'act out your dreams' while asleep (for example, punching, flailing your arms in the air, making running movements, etc.)?" Exclusion Criteria: - Existence of cognitive decline hard to participate in the clinical trial - Subject has confusion or visual hallucination in daytime - Diagnosed as obstructive sleep apnea or severe snoring - Previous clonazepam treatment within 4 weeks - Current treatment with benzodiazepines at bedtime - Alcoholics or drug abuser - Lactating, pregnant, or possible pregnant - Hypersensitivity to clonazepam or benzodiazepines - Prior participation to other clinical trials within 3 months - Presence of severe comorbidities or a cancer - Existence of illness or problems which makes difficult to be enrolled to this trial judged by clinicians |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Seoul National University Hospital | Seoul |
Lead Sponsor | Collaborator |
---|---|
Seoul National University Hospital | Ministry of Food and Drug Safety, Korea |
Korea, Republic of,
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Kunz D, Mahlberg R. A two-part, double-blind, placebo-controlled trial of exogenous melatonin in REM sleep behaviour disorder. J Sleep Res. 2010 Dec;19(4):591-6. doi: 10.1111/j.1365-2869.2010.00848.x. — View Citation
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Postuma RB, Arnulf I, Hogl B, Iranzo A, Miyamoto T, Dauvilliers Y, Oertel W, Ju YE, Puligheddu M, Jennum P, Pelletier A, Wolfson C, Leu-Semenescu S, Frauscher B, Miyamoto M, Cochen De Cock V, Unger MM, Stiasny-Kolster K, Fantini ML, Montplaisir JY. A single-question screen for rapid eye movement sleep behavior disorder: a multicenter validation study. Mov Disord. 2012 Jun;27(7):913-6. doi: 10.1002/mds.25037. Epub 2012 May 30. — View Citation
Postuma RB, Bertrand JA, Montplaisir J, Desjardins C, Vendette M, Rios Romenets S, Panisset M, Gagnon JF. Rapid eye movement sleep behavior disorder and risk of dementia in Parkinson's disease: a prospective study. Mov Disord. 2012 May;27(6):720-6. doi: 10.1002/mds.24939. Epub 2012 Feb 9. — View Citation
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* Note: There are 11 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Clinical Global Impression-Improvement scale (CGI-I) | Clinician assessed rating scale of clinical improvement or worsening relative to a baseline state, scored as 1, very much improved; 2, much improved; 3, minimally improved; 4, no change; 5, minimally worse; 6, much worse; or 7, very much worse. | Four weeks (plus or minus 3 days) | No |
Secondary | Clinical Global Impression-Severity scale (CGI-S) | Four weeks (plus or minus 3 days) | No | |
Secondary | Epworth Sleepiness Scale (ESS) | Four weeks (plus or minus 3 days) | No | |
Secondary | Parkinson Disease Sleep Scale (PDSS) | Four weeks (plus or minus 3 days) | No | |
Secondary | Montreal Cognitive Assessment (MoCA) | Four weeks (plus or minus 3 days) | No | |
Secondary | Unified Parkinson's Disease Rating Scale (UPDRS) | Four weeks (plus or minus 3 days) | No |
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