| Methods |
Randomised controlled parallel group study. Study duration 2 weeks. Multicentre Japanese study
No intention to treat analysis. |
| Participants |
225 patients (117 male, 78 female)
Inclusion criteria: age >20, pollakisuria, ability to record frequency/volume chart.
Exclusion criteria: Bladder outflow obstruction, UTI, Bladder necrosis, glaucoma. |
| Interventions |
Group 1: (n=99) Flavoxate 600mg daily
Group 2: (n=96) Propantheline 20mg daily |
| Outcomes |
Subjective symptom assessment, patients impressions, efficacy and uselfulness |
| Notes |
Translated Japanese trial. |
| Risk of bias |
| Bias |
Authors' judgement |
Support for judgement |
| Allocation concealment? |
Low risk |
A ‐ Adequate |
