Clinical Trials Directory

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UnknownNCT04703127

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.

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Sohag University · Academic / Other
Sex
Male
Age
20 Years – 50 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGTadalafil and Combined DapoxietineGroup 1 was given on-demand 30 mg dapoxetine and 10 mg tadalafil 1 h before intercourse.
DRUGDapoxietine and Combined Lidocaine 5% SprayGroup 2 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.

Timeline

Start date
2020-03-30
Primary completion
2021-01-30
Completion
2021-01-30
First posted
2021-01-11
Last updated
2021-01-11

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04703127. Inclusion in this directory is not an endorsement.