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The main goals were to compare the effectiveness of extracts of the plant Tribulus terrestris (TT; marketed as Tribestan), in comparison with placebo, for the treatment of guys with erectile dysfunction (ED) and with or without hypoactive libido disorder (HSDD), as well as to monitor the safety profile of the drug.

Phase IV, potential, randomized, double-blind, placebo-controlled scientific trial in parallel groups. This study included 180 males aged between 18 and 65 years with moderate or moderate ED and with or without HSDD: 90 were randomized to TT and 90 to placebo. Clients with ED and high blood pressure, diabetes mellitus, and metabolic syndrome were consisted of in the study.

Tribestan (Tribulus terrestris) 250mg *60 folm coated tablets by Sopharma

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Each Tribestan film-coated tablet consists of the active compound Tribulus terrestris, herba extractum siccum (35-45:1) 250mg which is standardized to furostanol saponins (not less than 112. 5mg). Each client received orally 32 film-coated tablets daily after meals, throughout the 12-week treatment duration. At the end of every month, individuals' sexual function, consisting of ED, was evaluated by International Index of Erectile Function (IIEF) Questionnaire and Worldwide Effectiveness Concern (GEQ).

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The main result measure was the change in IIEF score after 12 weeks of treatment. tribestan worldwide (random sorting using maximum allowable% deviation) with an equal variety of clients in each series was used. This randomization algorithm has the constraint that unequal treatment allowance is not allowed; that is, all groups should have the same target sample size.

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All outcome assessors were likewise blinded to group allowance. 86 patients in each group completed the research study. The IIEF rating improved substantially in the TT group compared with the placebo group (