Premature Ejaculation Clinical Trial
— PEOfficial title:
Evaluation of the Clinical Efficacy and Safety of Dapoxetine, Combined Dapoxetine With Folic Acid and Combined Dapoxetine With Vitamin B12 in Treatment of Patients With Premature Ejaculation: A Randomized Placebo-controlled Clinical Trial
Verified date | August 2019 |
Source | Sohag University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study will aim to assess of the clinical efficacy and safety of dapoxetine, combined dapoxetine with folic acid and combined dapoxetine with vitamin B12 in treatment of patients with premature ejaculation: A randomized placebo-controlled clinical trial.
Status | Completed |
Enrollment | 120 |
Est. completion date | August 29, 2019 |
Est. primary completion date | June 1, 2019 |
Accepts healthy volunteers | No |
Gender | Male |
Age group | 20 Years to 50 Years |
Eligibility |
Inclusion Criteria: Premature ejaculation Exclusion Criteria: - Erectile dysfunction - Diabetes mellitus - chronic prostatitis - Advanced renal or hepatic diseases - Neurological diseases |
Country | Name | City | State |
---|---|---|---|
Egypt | Faculty of Medicine, Sohag University, Egypt | Sohag |
Lead Sponsor | Collaborator |
---|---|
Sohag University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Arabic Index of Premature Ejaculation | The AIPE questionnaire includes seven questions.Response to each question will be scored on a scale from 1 to 5. | 0-6 weeks after treatment | |
Primary | Intravaginal ejaculatory latency times | By using stopwatches | 0-6 weeks after treatment |
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