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Clinical Trial Summary

The objective of this clinical trial is to evaluate the effectiveness and safety of transcutaneous posterior tibial nerve stimulation therapy in patients with premature ejaculation. The main question to answer is: Can the effectiveness and safety of transcutaneous electrostimulation of the posterior tibial nerve alone and combined with standard pharmacological treatment be evaluated in men with lifelong premature ejaculation, compared to standard pharmacological treatment with dapoxetine? Patients will: Be randomized in acontrolled clinical trial. Patients with a diagnosis of premature ejaculation who attend Boston Medical Group clinics in Mexico City will be included. Be assigned by randomization to one of three treatment groups: - Group 1: Tens therapy + dapoxetine placebo on demand. - Group 2: Standard treatment (dapoxetine 30 mg as needed) + placebo therapy. - Group 3: Tens therapy + standard treatment (dapoxetine 30 mg as needed).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06425224
Study type Interventional
Source Boston Medical Group
Contact Carolina Sandoval, Master
Phone +573133920816
Email csandoval@bostonmedical.com.co
Status Recruiting
Phase Phase 3
Start date June 15, 2022
Completion date June 2025

See also
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