Study design, materials and methods
It was a randomised crossover study (CTRI/2022/05/042706) with 20 patients in each group. Group 1 received Alfuzosin & Amitryptylin (AA) and group 2 received Yoga & Placebo (YP) for six weeks. After the end of six weeks, a washout period of one week was given and the crossover was done. The change in NIHCPSI scores was noted and compared using SPSS and R software.
Interpretation of results
Both groups had similar efficacy in decreasing symptoms of the CPPS patient. In subset analysis, the urinary symptoms scores responded to medical management rather than yoga. other symptoms reduced in both the groups without any significant difference.