Parkinson's Disease Clinical Trial
Official title:
Multicenter, Placebo Controlled, Randomized, Double-Blinded Study: Coenzyme Q10 Nanodispersion Versus Placebo as Symptomatic Treatment in Parkinson's Disease
This study was designed to evaluate the symptomatic effects of Coenzyme Q10 nanodispersed
solution in middle-stage Parkinson's disease (PD) patients (Hoehn&Yahr II to III). The
treatment phase includes three months period of 300 mg Coenzyme Q10 per day or placebo.
The primary outcome measure was the combined Unified Parkinson's Disease Rating Scale
(UPDRS) Part II and III.
The hypothesis of this study was that Coenzyme Q10 improves the energy status of the
diseased dopaminergic neuronal cell type and thus producing more dopamine leading to an
improvement of parkinsonian symptoms in PD patients.
| Status | Completed |
| Enrollment | 132 |
| Est. completion date | June 2005 |
| Est. primary completion date | June 2005 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 40 Years to 75 Years |
| Eligibility |
Inclusion Criteria: - Parkinson's disease according to the UK Brain Bank criteria - Hoehn & Yahr stadium II until III - Male or female - Age 40 to 75 years - UPDRS Part III > 15 points - No motor fluctuations or dyskinesias - Stable parkinsonian condition for 4 weeks prior to inclusion - Outpatients - Patients without or with stable levodopa treatment for 4 weeks prior inclusion - Written informed consent Exclusion Criteria: - Atypical or drug-induced parkinsonian syndromes - Dyskinesias or motor fluctuations - Coenzyme Q10 treatment in the past - Pregnancy - Epileptic seizures in the history - Hypothyroidism - Severe medical conditions with interference with study drug - Treatment with CSE inhibitors, thyroidal hormones, antiarrhythmic drugs, warfarin, metformin - Treatment or intake of vitamins, magnesium, vitamin E, calcium |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Germany | Department of Neurology, Charite Berlin | Berlin | |
| Germany | Department of Neurology, Ruhr-University of Bochum | Bochum | Nordrhein-Westfalen |
| Germany | Department of Neurology, Technical University of Dresden | Dresden | Saxony |
| Germany | Department of Neurology, Klinikum Essen-Borbeck | Essen | Nordrhein-Westfalen |
| Germany | Department of Neurology, Klinik Ambrock | Hagen | Nordrhein-Westfalen |
| Germany | Department of Neurology, University of Homburg | Homburg | Saarland |
| Germany | Department of Neurology, Fachklinik Ichenhausen | Ichenhausen | Bavaria |
| Germany | Department of Nuerology, Klinikum Lippe | Lemgo | Niedersachsen |
| Germany | Department of Neurology, Klinikum Lueneburg | Lueneburg | Niedersachsen |
| Germany | Department of Neurology, University of Marburg | Marburg | Hessen |
| Germany | Department of Neurology, Leopoldina Krankenhaus | Schweinfurt | Bavaria |
| Germany | Department of Neurology, University of Ulm | Ulm | Baden-Württemberg |
| Germany | Department of Neurology, Deutsche Klinik fuer Diagnostik | Wiesbaden | Hessen |
| Lead Sponsor | Collaborator |
|---|---|
| Technische Universität Dresden | Deutsche Parkinson-Vereinigung e.V., MSE Pharmazeutika GmbH, Bad Homburg |
Germany,
Storch A, Jost WH, Vieregge P, Spiegel J, Greulich W, Durner J, Müller T, Kupsch A, Henningsen H, Oertel WH, Fuchs G, Kuhn W, Niklowitz P, Koch R, Herting B, Reichmann H; German Coenzyme Q(10) Study Group. Randomized, double-blind, placebo-controlled tria — View Citation
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Unified Parkinson's Disease Rating Scale (UPDRS) Part II and III | |||
| Secondary | Total UPDRS | |||
| Secondary | Safety | |||
| Secondary | PDQ-39 | |||
| Secondary | SF36 | |||
| Secondary | CGI | |||
| Secondary | Schwab&England | |||
| Secondary | Montgomery-Asperg | |||
| Secondary | Pain | |||
| Secondary | Incontinence | |||
| Secondary | Sexual behavior |
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