FREEDOM - First Real-Life Evaluation of Enablex Done in ZA Overactive Bladder Patients During a 3 Months Period

NCT00921245 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 9

Last updated 2015-04-20

No results posted yet for this study

Summary

Patient perspective on Overactive Bladder and symptoms experienced after administration of Darifenacin

Conditions

Interventions

DRUG

Darifenacin (Emselex, BAY79-4998)

Patients in daily clinical treatment receiving Emselex according to local drug information

Sponsors & Collaborators

Principal Investigators

  • Bayer Study Director · Bayer

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-06-30
Primary Completion
2008-10-31
Completion
2009-02-28

Countries

  • South Africa

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00921245 on ClinicalTrials.gov