Toviaz Post Marketing Surveillance Study

Pfizer

Status: Completed

Conditions: Overactive Bladder

Treatments: Drug: Toviaz treatment

Study type: Observational

Funder types: Industry

Identifiers

NCT00879398

A0221075

Details and patient eligibility

About

The objective of this study is to determine the problems and questions of safety and efficacy of Toviaz® under the standard conditions of usage.

Full description

continuous registration method

Enrollment: 3,000 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Subjects who are diagnosed as Overactive Bladder (OAB) defined as urgency, with or without urgency incontinence, usually with frequency and nocturia, in the absence of local or metabolic factors explaining these factors.

Exclusion criteria

• Hypersensitivity to the active substance or to peanut or soya or any of the excipients
• Urinary retention
• Gastric retention
• Uncontrolled narrow angle glaucoma
• Myasthenia gravis
• Severe hepatic impairment (Child Pugh C)
• Concomitant use of potent CYP3A4 inhibitors in subjects with moderate to severe hepatic or renal impairment
• Severe ulcerative colitis
• Toxic megacolon
• Patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption (Toviaz® prolonged-release tablets contain lactose)

Trial design

3,000 participants in 1 patient group

OAB-Toviaz

Description:

All patients who enrolled in this study

Treatment:

Drug: Toviaz treatment