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Clinical Trial Summary

Therefore, this study will aim to assess the effectiveness and tolerability of the on-demand use of combined dapoxetine with tadalafil and combined dapoxetine with lidocaine 5% spray in treatment of patients with lifelong premature ejaculation and non-responding to dapoxetine alone.


Clinical Trial Description

This study will be carried out on 60 patients with lifelong premature ejaculation and non-responding to dapoxetine alone. All patients will be equally divided into 2 groups (30 patients each). Group 1 was given on-demand 30 mg dapoxetine and 10 mg tadalafil 1 h before intercourse. Group 1 was given on-demand 30 mg dapoxetine 1 h before intercourse and apply lidocaine 5% spray on the glans penis 10 minutes the wash before intercourse. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04703127
Study type Interventional
Source Sohag University
Contact Mohammed A Abu El-Hamd, MD
Phone 01004139060
Email Mohammedadva@yahoo.com
Status Recruiting
Phase Phase 3
Start date March 30, 2020
Completion date January 30, 2021

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