NCT01091519

Non-Interventional Study To Investigate Whether Information Provided To Patients Influences Their Satisfaction With Toviaz Therapy

Facts Study (Fakten-studie): Non-interventional Study to Investigate Whether Information Provided to Patients Influences Satisfaction With Toviaz Therapy As Perceived by the Patient

• Status: Terminated
• Phase: —
• Study type: Observational
• Enrollment: 781 (actual)
• Sponsor: Pfizer · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

Collect information on treatment with Toviaz (fesoterodine) under ordinary prescribing conditions, and to investigate whether additional educational information affects satisfaction with treatment as perceived by the patient.

Detailed description

Patients will be identified and monitored during routine clinical practice visits, and will not be specifically selected as this would interfere with the representativeness of the results. The study will be conducted with office-based urologists and office-based general physicians, practitioners and internists (GPs) in Germany, thus representing a wide range of practices and populations. Each urologist or GP may invite patients to participate who have already been diagnosed with overactive bladder and prescribed Toviaz according to their usual standard of care. Study enrollment stopped on December 31, 2011 due to difficulty in recruiting patients. No safety issues were related to the decision to stop patient enrollment.

Conditions

• Urinary Bladder, Overactive

Interventions

Type	Name	Description
OTHER	Toviaz(fesoterodine) plus educational materials	Educational materials including the Self-Assessment Goal Achievement (SAGA) tool to support dialogue.
OTHER	Toviaz(fesoterodine) without educational materials	No educational materials

Timeline

• Start date: 2010-12-01
• Primary completion: 2012-05-01
• Completion: 2012-05-01
• First posted: 2010-03-24
• Last updated: 2013-03-07
• Results posted: 2013-03-07