Evaluation of patients' satisfaction with the effectiveness of dopoxetin in premature ejaculation and its complications
- Conditions
- Premature ejaculation.Premature ejaculationF52.4
- Registration Number
- IRCT20200624047912N1
- Lead Sponsor
- Islamic Azad University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Male
- Target Recruitment
- 100
Have ejaculatory ejaculation
Be at least 20 to 40 years old
Tendency to take medications regularly and continuously until the end of the treatment period
Have a desire to participate and cooperate in this research 5. Have at least once a week close
Do not have any contraindications to the use of drugs (sensitivity to SSRI_ alcohol consumption_ calculation of lactose_ history of heart problem_depression) You have become _strength of safety_consumption of tramadol_ _MAOI
Have no history of drug and alcohol use continuously
Disorder of erection, genital urinary tract infection, systemic or neurological disorder, do not have severe mental disorder
Do not have a history of IHD, DM, HTN, HLP and severe vascular disorders as proven
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Ejaculation time. Timepoint: Before treatment - 10 days after treatment - one month later. Method of measurement: Questionnaires 1, 2 and 3whith Using a timer to minute.;Drug side effects. Timepoint: 10 days after treatment - one month later. Method of measurement: Questionnaires 2 and 3 mention the specified options.;Satisfaction with treatment. Timepoint: 10 days after treatment - one month later. Method of measurement: Questionnaires 2 and 3 mention excellent, good, medium, poor.
- Secondary Outcome Measures
Name Time Method Ejaculation time score. Timepoint: Before treatment - 10 days after treatment - one month later. Method of measurement: Questionnaires 1, 2 and 3 with the option marked to the time score.