Reproducibility Study of Over Active Bladder Symptom Score [OABSS]

The purpose of this study is to evaluate the reproducibility of over active bladder symptom score (OABSS) in Asian countries.

Completed

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Key information

Conditions

Overactive Bladder Female Urogenital Diseases Female Urogenital Diseases and Pregnancy Complications Lower Urinary Tract Symptoms Male Urogenital Diseases Pathological Conditions, Signs and Symptoms Signs and Symptoms Urinary Bladder Diseases Urinary Bladder, Overactive Urogenital Diseases Urologic Diseases Urological Manifestations

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Beijing, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Symptoms OAB for 3 months or longer
At least 1 urgency episode in last 3 days
Symptoms of OAB as verified by the screening 3-day bladder diary, defined by:

Number of micturition ≥8 times/day
Number of urgency episode in 3 days ≥1

Exclusion criteria

Indwelling catheters or practicing intermittent self-catheterization
Symptomatic urinary tract infection, chronic inflammation
Diabetic neuropathy

Treatment and study plan

Primary outcomes

OABSS

Time frame: Weeks of 0 and 2

Secondary outcomes

3-day micturition diary

Time frame: 2 times in 2-week interval

Sponsors and collaborators

Lead sponsor

Astellas Pharma Inc

Industry

Collaborators

Astellas Pharma China, Inc.

Registry information

Official study title

Reproducibility Study of OABSS and Its Response to Treatment - Part 1: Reproducibility -

Acronym: RESORT

Important dates

Study start: 2009
Primary completion: 2009
Study completion: 2009
First posted: May 13, 2009
Registry last updated: Mar 15, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed