Materials-methods
The current study was designed as a prospective and randomised experimental study. The study was approved by Kutahya Health Sciences University Ethical Committee on 08.07.20 with 2020-04/10 decision number.
Patients diagnosed with refractory OAB-wet type were included study according to inclusion and exclusion criteria (Table-1). Sixty patients included in the study were randomly divided into two groups using a simple random number table after informed consent form as established for each participant. Our study was prepared in accordance with the CONSORT guide (15). The CONSORT study flow chart was prepared (Figure-1).