Reproducibility Study of Overactive Bladder Symptom Score [OABSS] (RESORT-1)

Astellas

Status: Completed

Conditions: Overactive Bladder

Study type: Observational

Funder types: Industry

Identifiers

NCT01122550

EQL-CRU.004-2009

Details and patient eligibility

About

The purpose of this study is to evaluate its reproducibility of overactive bladder symptom score (OABSS) and to evaluate its correlation to other measures of OAB symptoms.

Enrollment: 50 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Symptoms OAB for 3 months or longer

• At least 1 urgency episode in last 3 days

• Symptoms of OAB as verified by 3-day micturition diary prior to Visit 1, defined by:

  • Number of micturition per day ≥8
  • Number of urgency episodes in 3 days ≥1

Exclusion criteria

• Significant stress incontinence or mixed stress/urge incontinence
• Subjects with indwelling catheters or practicing intermittent self-catheterization
• Symptomatic urinary tract infection, chronic inflammation
• Diabetic neuropathy
• Drug or non-drug treatment for OAB was started, quitted or changed in 4 weeks
• Participation in any clinical trial in 30 days