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BI_Sifrol Tablets Special Drug Use Surveillance(Survey on the Safety and Efficacy in Parkinson's Disease Patients With Depressive Symptoms)
The primary objective of this investigation is to conduct a 12-week prospective survey in PD patients with depressive symptoms treated with BI Sifrol Tablets (hereinafter referred to as this drug) in the routine clinical settings to determine the following items related to the safety and efficacy. i. Adverse drug reaction symptoms, incidence, and severity ii. Motor capacity during the investigation iii. Depressive symptoms during the investigation
Age
20 - No limit years
Sex
ALL
Healthy Volunteers
No
Boehringer Ingelheim Investigational Site
Akashi, Japan
Boehringer Ingelheim Investigational Site 1
Akita, Japan
Boehringer Ingelheim Investigational Site 2
Akita, Japan
Boehringer Ingelheim Investigational Site
Asahikawa, Japan
Boehringer Ingelheim Investigational Site
Ashikaga, Japan
Boehringer Ingelheim Investigational Site
Awaji, Japan
Boehringer Ingelheim Investigational Site
Chitose, Japan
Boehringer Ingelheim Investigational Site
Chūō, Japan
Boehringer Ingelheim Investigational Site 1
Fuchū, Japan
Boehringer Ingelheim Investigational Site 2
Fuchū, Japan
Start Date
January 1, 2007
Primary Completion Date
August 1, 2009
Last Updated
August 6, 2014
1,089
ACTUAL participants
Lead Sponsor
Boehringer Ingelheim
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06113640