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).