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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.

Register:	ClinicalTrials.gov
Last refreshed on:	19 October 2017
Main ID:	NCT00802178
Date of registration:	03/12/2008
Prospective Registration:	No
Primary sponsor:	Boehringer Ingelheim
Public title:	First Presentation of Parkinson Disease Patients to Neurologist
Scientific title:	CEE PMSS (Central Eastern European Post-Marketing Surveillance Study) First Presentation of Mirapexin in Parkinson Patients
Date of first enrolment:	February 2006
Target sample size:	2448
Recruitment status:	Completed
URL:	https://clinicaltrials.gov/show/NCT00802178
Study type:	Observational
Study design:
Phase:	N/A

Countries of recruitment
Croatia	Czech Republic	Estonia	Hungary	Romania	Russian Federation	Serbia	Slovakia
Slovenia

Contacts

Name:	Boehringer Ingelheim
Address:
Telephone:
Email:
Affiliation:	Boehringer Ingelheim

Key inclusion & exclusion criteria

Inclusion Criteria:

- Parkinson Disease patients presenting to neurologist for first time

Exclusion Criteria:

- Hypersensitivity to the active substance or to any of the excipients

Age minimum: 18 Years
Age maximum: N/A
Gender: All

Health Condition(s) or Problem(s) studied

Parkinson Disease

Intervention(s)

Primary Outcome(s)

Number of De-novo Patients in Whom Monotherapy With Mirapexin® Could be Successfully Initiated [Time Frame: 4 - 8 weeks]

Secondary Outcome(s)

Change From Baseline in UPDRS (Unified Parkinson's Disease Rating Scale) Part I [Time Frame: Baseline and 4 to 8 weeks]

Global Clinical Assessments of Efficacy of Mirapexin® for All Patients [Time Frame: 4 - 8 weeks]

Change From Baseline in UPDRS Part III [Time Frame: Baseline and 4 - 8 weeks]

Secondary ID(s)

248.613

Source(s) of Monetary Support

Please refer to primary and secondary sponsors

Secondary Sponsor(s)

Ethics review

Results

Results available:	Yes
Date Posted:	20/11/2009
Date Completed:
URL:	https://clinicaltrials.gov/ct2/show/results/NCT00802178

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