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Influence of Lisdexamfetamine Dimesylate on Early Ejaculation—Results from a Double-Blind Randomized Clinical Trial

Background: Among male sexual dysfunctions, erectile dysfunction and early ejaculation have the highest prevalence rates. Here, we tested the influence of lisdexamfetamine dimesylate (Vyas(®)) on early ejaculation. To this end, we performed a double-blind randomized clinical trial among males with e...

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Autores principales: Haghighi, Mohammad, Doostizadeh, Mona, Jahangard, Leila, Soltanian, Alireza, Faryadres, Mohammad, Dürsteler, Kenneth M., Beatrix Brühl, Annette, Sadeghi-Bahmani, Dena, Brand, Serge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8303163/
https://www.ncbi.nlm.nih.gov/pubmed/34356237
http://dx.doi.org/10.3390/healthcare9070859
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author Haghighi, Mohammad
Doostizadeh, Mona
Jahangard, Leila
Soltanian, Alireza
Faryadres, Mohammad
Dürsteler, Kenneth M.
Beatrix Brühl, Annette
Sadeghi-Bahmani, Dena
Brand, Serge
author_facet Haghighi, Mohammad
Doostizadeh, Mona
Jahangard, Leila
Soltanian, Alireza
Faryadres, Mohammad
Dürsteler, Kenneth M.
Beatrix Brühl, Annette
Sadeghi-Bahmani, Dena
Brand, Serge
author_sort Haghighi, Mohammad
collection PubMed
description Background: Among male sexual dysfunctions, erectile dysfunction and early ejaculation have the highest prevalence rates. Here, we tested the influence of lisdexamfetamine dimesylate (Vyas(®)) on early ejaculation. To this end, we performed a double-blind randomized clinical trial among males with early ejaculation. Methods: A total of 46 males with early ejaculation (mean age: 35.23 years) and in stable marital relationships with regular weekly penile–vaginal intercourse were randomly assigned either to the lisdexamfetamine dimesylate condition (30 mg) or to the placebo condition. Compounds were taken about six hours before intended penile–vaginal intercourse. At baseline and four weeks later at the end of the study, participants completed a series of self-rating questionnaires covering early ejaculation. Female partners also rated participants’ early ejaculation profile. Results: Compared to the placebo condition, dimensions of early ejaculation improved over time in the lisdexamfetamine condition, though improvements were also observed in the placebo condition. Conclusions: Among male adults in stable marital relationships with regular weekly penile–vaginal intercourse, lisdexamfetamine dimesylate improved dimensions of early ejaculation. Given that improvements were also observed in the placebo condition, psychological factors such as increased attention to early ejaculation and favorable expectations of the compound should be considered.
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spelling pubmed-83031632021-07-25 Influence of Lisdexamfetamine Dimesylate on Early Ejaculation—Results from a Double-Blind Randomized Clinical Trial Haghighi, Mohammad Doostizadeh, Mona Jahangard, Leila Soltanian, Alireza Faryadres, Mohammad Dürsteler, Kenneth M. Beatrix Brühl, Annette Sadeghi-Bahmani, Dena Brand, Serge Healthcare (Basel) Article Background: Among male sexual dysfunctions, erectile dysfunction and early ejaculation have the highest prevalence rates. Here, we tested the influence of lisdexamfetamine dimesylate (Vyas(®)) on early ejaculation. To this end, we performed a double-blind randomized clinical trial among males with early ejaculation. Methods: A total of 46 males with early ejaculation (mean age: 35.23 years) and in stable marital relationships with regular weekly penile–vaginal intercourse were randomly assigned either to the lisdexamfetamine dimesylate condition (30 mg) or to the placebo condition. Compounds were taken about six hours before intended penile–vaginal intercourse. At baseline and four weeks later at the end of the study, participants completed a series of self-rating questionnaires covering early ejaculation. Female partners also rated participants’ early ejaculation profile. Results: Compared to the placebo condition, dimensions of early ejaculation improved over time in the lisdexamfetamine condition, though improvements were also observed in the placebo condition. Conclusions: Among male adults in stable marital relationships with regular weekly penile–vaginal intercourse, lisdexamfetamine dimesylate improved dimensions of early ejaculation. Given that improvements were also observed in the placebo condition, psychological factors such as increased attention to early ejaculation and favorable expectations of the compound should be considered. MDPI 2021-07-07 /pmc/articles/PMC8303163/ /pubmed/34356237 http://dx.doi.org/10.3390/healthcare9070859 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Haghighi, Mohammad
Doostizadeh, Mona
Jahangard, Leila
Soltanian, Alireza
Faryadres, Mohammad
Dürsteler, Kenneth M.
Beatrix Brühl, Annette
Sadeghi-Bahmani, Dena
Brand, Serge
Influence of Lisdexamfetamine Dimesylate on Early Ejaculation—Results from a Double-Blind Randomized Clinical Trial
title Influence of Lisdexamfetamine Dimesylate on Early Ejaculation—Results from a Double-Blind Randomized Clinical Trial
title_full Influence of Lisdexamfetamine Dimesylate on Early Ejaculation—Results from a Double-Blind Randomized Clinical Trial
title_fullStr Influence of Lisdexamfetamine Dimesylate on Early Ejaculation—Results from a Double-Blind Randomized Clinical Trial
title_full_unstemmed Influence of Lisdexamfetamine Dimesylate on Early Ejaculation—Results from a Double-Blind Randomized Clinical Trial
title_short Influence of Lisdexamfetamine Dimesylate on Early Ejaculation—Results from a Double-Blind Randomized Clinical Trial
title_sort influence of lisdexamfetamine dimesylate on early ejaculation—results from a double-blind randomized clinical trial
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8303163/
https://www.ncbi.nlm.nih.gov/pubmed/34356237
http://dx.doi.org/10.3390/healthcare9070859
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