CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 908 enrolled
Drug / intervention
piribedil (Clarium)drug
Likely dose
piribedil (Clarium) 50 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01519856
NCT01519856N/ACompleted

Efficacy and Safety of Long-term Therapy With Piribedil (CLARIUM) in Patients With M. Parkinson Under Consideration of Quality of Life Parameters and Cognitive Function

Desitin Arzneimittel GmbH·observational·Posted Jan 27, 2012·Updated Jan 29, 2016

In Brief

An observational study evaluating piribedil (Clarium) for Parkinson's Disease. Completed, enrolled 908 participants across 1 site.

Detailed Summary

Non-Ergot Dopamine agonists are meanwhile the drugs of first-choice in the treatment of Parkinson's disease. The receptor profile of the non-ergot dopamine-agonist piribedil is unique. In addition to agonistic effects on dopaminergic D2- and D3-receptors piribedil has adrenergic alpha-2A- and alpha-2C-receptors antagonisic properties. There is evidence from the literature that the antagonistic properties of piribedil are correlated with an improvement of cognitive function and vigilance parameters in parkinson's disease. The aim of the present non-interventional study is to investigate the safety and efficacy of piribedil during long-term therapy of patients with M. Parkinson under consideration of cognitive functions and quality of life.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesGermany
Collaborators--

Timeline

N/ACompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedJan 27, 2012
Enrollment StartJun 1, 2009
Primary CompletionDec 1, 2014
Study CompletionFeb 1, 2015
TodayJul 2, 2026
Enrollment to primary: 5.5 yearsPosted 14.4 years ago

Interventions

piribedil (Clarium)drug

oral tablets, 50 mg