J Sex Med. 2010 Jan;7(1 Pt 2):414-44. doi: 10.1111/j.1743-6109.2009.01623.x.
Clinical trials in male sexual dysfunction (MSD) are expanding. Consequently, there is a need for consensus standards in this area.
To develop an evidence-based, state-of-the-art consensus report on standards for clinical trials in MSD.
A literature review was performed examining clinical trials in erectile dysfunction (ED), premature ejaculation (PE), delayed/absent ejaculation, libido disorders/loss of desire, hypogonadism, and Peyronie's disease, focusing on publications published in the last 20 years. This manuscript represents the opinions of eight experts from seven countries developed in a consensus process. This document was presented for peer review and debate in a public forum and revisions were made based on recommendations of chairpersons to the International Consultation on Sexual Medicine.
Expert opinion was based on the grading of evidence-based medical literature, widespread internal committee discussion, public presentation, and debate.
According to experience and recent publications in dealing with clinical trials in sexual dysfunction, recommendations have been made for conducting trials in patients with ED, PE, delayed ejaculation, libido disorders, hypogonadism, and Peyronie's disease.
It is important that future clinical trials are conducted using standards upon which investigators can rely when reading manuscripts or conducting new trials in this field.
男性性功能障碍(MSD)的临床试验正在不断扩展。因此,该领域需要有共识标准。
制定基于证据的、最新的 MSD 临床试验标准共识报告。
对勃起功能障碍(ED)、早泄(PE)、延迟/无射精、性欲障碍/性欲减退、性腺功能减退和佩罗尼氏病的临床试验进行了文献回顾,重点关注过去 20 年发表的出版物。本文档代表了来自七个国家的八位专家在共识过程中形成的意见。本文件在公开论坛上进行了同行评议和辩论,并根据主席对国际性医学咨询的建议进行了修订。
专家意见基于循证医学文献的分级、广泛的内部委员会讨论、公开陈述和辩论。
根据处理性功能障碍临床试验的经验和最近的出版物,我们提出了 ED、PE、延迟射精、性欲障碍、性腺功能减退和佩罗尼氏病患者临床试验的建议。
未来的临床试验使用研究人员在阅读文献或在该领域开展新试验时可以依赖的标准进行非常重要。