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Клинические исследования в Украине

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Описание
Краткое названиеClinical Trial to Evaluate the Efficacy and Safety of Fesoterodine in Comparison to Tolterodine for Overactive Bladder (OAB)
Полное название12-Week, Randomized, Double-Blind, Double-Dummy,Placebo-Controlled, Parallel-Group, Multicenter Trial To Evaluate The Efficacy And Safety Of Fesoterodine In Comparison To Tolterodine ER In Patients With Overactive Bladder (OAB)
СпонсорPfizer
Industry
ИсточникPfizer
Под контролемUnited States: Food and Drug Administration
No
Краткое описаниеTo evaluate the efficacy and safety of fesoterodine in comparison to tolterodine and placebo
for overactive bladder
СостояниеЗавершено
Дата началаApril 2007
ФазаPhase 3
Вид исследованияAllocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment
Набор0
КритерииInclusion Criteria:

- Adult overactive bladder (OAB) patients who present with OAB symptoms, including
urinary frequency >= 8 per day and urgency urinary incontinence >=1 per day

Exclusion Criteria:

- Patients with conditions that would contraindicate for fesoterodine use, e.g,
hypersensitivity to the active substance (fesoterodine) or to peanut or soya or any
of the excipients, urinary retention, and gastric retention.

- Patients with significant hepatic and renal disease or other significant unstable
diseases.

- OAB symptoms caused by neurological conditions, known pathologies of urinary tract,
etc.
ПолBoth
Минимальный возраст18 Years
Максимальный возрастN/A
УсловиеOveractive Bladder
Применяемое лечение
Drugfesoterodine fumarate
Drugplacebo
Drugtolterodine tartrate
Контакты и расположение
Chernivtsi , 58002Pfizer Investigational Site
Kharkiv , 61037Pfizer Investigational Site
Kyiv , 04053Pfizer Investigational Site
Odessa , 65000Pfizer Investigational Site
Zaporizhzhia , 69000Pfizer Investigational Site
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