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At the baseline of the study and after 4-week treatment, all participants completed the questionnaires, including the NIH-CPSI and I-PSS for LUTS.[6–7] All subjects were assessed for total prostate volume (TPV) by trans-rectal ultrasonography (using Logiq 5 Pro by GENERAL ELECTRIC, Milwaukee, WI, USA) and for urinary flow rates by uroflowmetry (using Urodyn 1000 by MEDTRONIC, Minneapolis, MN, USA).
Copyright and License information: ©2018 Ausmees et al
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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