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. 2022 Jan 1;45(5):941–961. doi: 10.1007/s40618-021-01704-3

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© The Author(s) 2021

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — a Prevalence of patients without ED (blue dots), and of mild (white dots), mild–moderate (gray dots) and moderate (black dots) ED assessed by IIEF-6 questionnaire in l-arginine group at baseline (a1) vs 90 days (a2). b Prevalence of patients without vasculogenic ED (blue dots), and of mild–moderate (gray dots) and severe (black dots) vasculogenic ED assessed at dynamic PDU in l-arginine group at baseline (b1) vs 90 days (b2). c Prevalence of patients without ED (blue dots), and of mild (white dots), mild–moderate (gray dots) and moderate (black dots) ED assessed by IIEF-6 questionnaire in placebo group at baseline (c1) vs 90 days (c2). d Prevalence of patients without vasculogenic ED (blue dots), and of mild–moderate (gray dots) and severe (black dots) vasculogenic ED assessed at dynamic PDU in placebo group at baseline (d1) vs 90 days (d2)