尿失禁および腹圧性尿失禁の兆候を示す女性患者におけるプロピベリン塩酸塩の研究

基本情報

NCT ID: NCT01942681
ステータス: 完了
試験のフェーズ: 該当なし
試験タイプ: 介入
目標被験者数: 62
治験依頼者名: Translational Research Center for Medical Innovation, Kobe, Hyogo, Japan

概要

This study is to evaluate the efficacy and safety that the occurrence of incontinence is significantly decrease using the propiverine hydrochloride for 200 female patients with mixed (stress and urge) urinary incontinence in one week during a twelve-week treatment period.

対象疾患

Urinary Incontinence

介入

Propiverine Hydrochloride(DRUG)

依頼者（Sponsor）

Translational Research Center For Medical Innovation, Kobe, Hyogo, Japan(OTHER)

Shinshu University Hospital(UNKNOWN)

実施施設 (1)

信州大学医学部附属病院

Matsumoto, Nagano, Japan