The main objective of this study is to evaluate the response of erectile dysfunction in hypogonadotrophic males with Testosterone undecanoate i.m. as per IIEF and the question of the GAQ (Global Evaluation Questionnaire) after 42 weeks of treatment. Secondary Study Objectives * To monitor adverse events and changes in hemoglobin and serum chemistry with: PSA, lipid profile, renal-hepatic profile and glycemia, and control by means of a rectal digital examination. * To Determinate physiologic reconstitution in patients under treatment by means of total and free testosterone dosage.
The importance of testosterone in desire, interest and sexual motivation is well known, but its effects on erectile function continue provoking controversy. Data obtained in animals under experimental or surgical castration, explains how this condition can cause a veno-occlusive dysfunction and therefore an erectile dysfunction. In a model of animal flebogenous erectile dysfunction, the intracavernous vascular endothelial growth factor (VEGF), together with testosterone, reestablishes the balance between the muscle and the conjunctive tissue, hypertrophy and hyperplasia of endothelial cells and regularizes the diameter of dorsal nervous cells, thus preventing the veno-occlusive dysfunction. Castration also induces the apopthosis in the erectile tissue of the penis; the treatment with testosterone provokes a new DNA synthesis. There are certain indicators that the treatment with testosterone could help patients with erectile dysfunction and low testosterone base line amounts. Likewise, androgens could control the expression and the activity of type 5 phosphodiesterase (PDE-5) of the cavernous body of the penis. Pharmacological treatment with PDE-5 inhibitors, administered orally fails in certain cases of erectile dysfunction, even more in hypogonadal males. Some studies show that the combination of testosterone with a PDE-5 inhibitor helps the recovery of sexual function in patients; therefore, giving the possibility of a combined pharmacological treatment with testosterone in erectile dysfunction.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
50
Testosterone Undecanoate 1000 mg IM injection; PDF5 tab, 20 mg
Hospital Santa Fe
Mexico City, D.F., Mexico
NOT_YET_RECRUITINGHospital General de Occidente
Guadalajara, Jalisco, Mexico
RECRUITINGHospital General de Occidente
Guadalajara, Jalisco, Mexico
NOT_YET_RECRUITINGHospital Universitario de Nuevo León
Monterrey, Nuevo León, Mexico
NOT_YET_RECRUITINGScore higher than or equal to 21 of the erectile dysfunction domain of the IIEF, or response to treatment
Time frame: 42 weeks
and/or an affirmative response to the GAQ will be considered for the analysis
Time frame: 10 months
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