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| ID | Type | Description | Link |
|---|---|---|---|
| 34039/KA-OTKA/11-10 | Other Identifier | University of Pécs, Faculty of Medicine |
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Lack of financial support
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Aim of the study is to perform a double-blind, crossover, placebo-controlled multicenter study evaluating the efficacy of pramipexole on essential tremor.
Essential tremor is one of the most common movement disorders with the prevalence of 3-5% among the elderly population. Although its main clinical feature is the bilateral, predominantly postural-kinetic tremor, newer studies suggest that ET is a spectrum of clinical features with both motor and nonmotor elements not homogeneously distributed.
Despite its high occurrence, the pharmacological treatment of ET is limited. Although the mainline drugs, propranolol and primidone, can provide good clinical benefit in a portion of cases, >50% of the patients stop the medication due to inefficacy or side-effects. Hypotension, dizziness, bradycardia, cognitive impairment, fatigue and erectile dysfunction are the most common side-effects contributing to medication discontinuation.
In an open-label pilot study, the investigators previously demonstrated that 2.1 mg/day pramipexole extended-release improved both the severity of tremor (by 52%) and health-related quality of life.
The present study aims to confirm this hypothesis in a double-blind, crossover, placebo-controlled multicenter study.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Process 1 | Active Comparator | 10 weeks of pramipexole treatment 2 weeks wash-out period (cross-over) 10 weeks placebo treatment |
|
| Process 2 | Placebo Comparator | 10 weeks of placebo treatment 2 weeks wash-out period (cross-over) 10 weeks pramipexole treatment |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| pramipexole | Drug | pramipexole extended release, 2.1 mg pramipexole base (3.0mg pramipexole salt) once daily |
|
| Measure | Description | Time Frame |
|---|---|---|
| Improvement in tremor severity | Improvement in tremor severity measured by Fahn-Tolosa-Marin Tremor Rating Scale | 10 weeks of treatment |
| Measure | Description | Time Frame |
|---|---|---|
| Improvement in quality of life | Improvement in quality of life assessed by EQ-5D score | 10 weeks of treatment |
| Number of Participants with Adverse Events as a Measure of Safety and Tolerability |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Norbert Kovacs, MD, PhD | Associate professor | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Department of Neurology, University of Pécs | Pécs | Baranya | H-7623 | Hungary | ||
| Kaposi Mór County Hospital |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| Background | Kovács N, Pál E, Késmárky I, Komoly S, Nagy F, Herceg M. Pramipexole for treating essential tremor. Eur J Neurol 2011;18(Suppl 2):482. |
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| ID | Term |
|---|---|
| D020329 | Essential Tremor |
| ID | Term |
|---|---|
| D009069 | Movement Disorders |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
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| ID | Term |
|---|---|
| D000077487 | Pramipexole |
| ID | Term |
|---|---|
| D052160 | Benzothiazoles |
| D013844 | Thiazoles |
| D001393 | Azoles |
| D006573 | Heterocyclic Compounds, 1-Ring |
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| placebo | Drug | placebo |
|
| 10 weeks of treatment |
| Kaposvár |
| Somogy County |
| H-7400 |
| Hungary |
| D006571 |
| Heterocyclic Compounds |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |