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Post Marketing Surveillance Study on Emselex After Launch in Germany

NCT ID: NCT00786448

Last Updated: 2010-04-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

5821 participants

Study Classification

OBSERVATIONAL

Study Start Date

2005-01-31

Study Completion Date

2006-02-28

Brief Summary

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\- Data are obtained of Emselex in routine treatment of Overactive Bladder. The general objectives are to evaluate the product safety, compatibility, efficacy and patient acceptance.

Detailed Description

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Conditions

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Overactive Bladder

Keywords

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Overactive Bladder

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Group 1

Darifenacin, Emselex (BAY79-4998)

Intervention Type DRUG

Patients from routine practice

Interventions

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Darifenacin, Emselex (BAY79-4998)

Patients from routine practice

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Patients who are treated with Emselex for Overactive Bladder
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bayer

INDUSTRY

Sponsor Role lead

Responsible Party

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Bayer Schering Pharma AG

Principal Investigators

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Bayer Study Director

Role: STUDY_DIRECTOR

Bayer

Locations

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Many Locations, , Germany

Site Status

Countries

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Germany

Other Identifiers

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EX0501DE

Identifier Type: -

Identifier Source: secondary_id

12245

Identifier Type: -

Identifier Source: org_study_id