Premature ejaculation
Conditions
Interventions
Observation group:None
Sponsors
Zhongnan Hospital of Wuhan University
Eligibility
Sex/Gender
Male
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: Select outpatient patients from urology and urology departments who have been clinically diagnosed with premature ejaculation based on their chief complaint, physical examination, and auxiliary examinations, and voluntarily participate and sign an informed consent form 1.The enrolled patients are premature ejaculation patients 2.The patient is aged 18-50 years old and generally in good physical condition 3.The patient has a fixed sexual partner, has had regular sexual activity for more than six months, and has had six or more sexual activities in the past month; Ensure 1-2 sexual activities per week during the study period. 4.Diagnosis of primary premature ejaculation 5.Diagnosis of peripheral premature ejaculation: quantitative sensation threshold measurement or penile vibration threshold measurement
Exclusion criteria
Exclusion criteria: 1.Exclude those who have taken serotonergic active drugs (such as ketamine), SSRIs, TCA preparations, PDE5i, and those who must take the above drugs during the trial period within the 4 weeks prior to screening; 2.Exclude individuals with comorbidities of mental illness, cardiovascular and cerebrovascular diseases, liver and kidney dysfunction, and alcohol dependence; 3.Exclude individuals with erectile dysfunction (assessed using the IIEF-5 scoring system for erectile function); 4.Individuals known to be allergic to the study drug and its excipient components
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intravaginal ejaculation latency, IELT; | — |
Secondary
| Measure | Time frame |
|---|---|
| Diagnostic tools for premature ejaculation, PEDT;Penile erectile function score, IIEF-5; | — |
Countries
China
Contacts
Public ContactSu Xinjun
Zhongnan Hospital of Wuhan University
Outcome results
None listed