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Transcutaneous Electrical Nerve Stimulation for in the Treatment of Premature Ejaculation

Not Applicable
Completed
Conditions
Transcutaneous Electrical Nerve Stimulation
Premature Ejaculation
Registration Number
NCT06570512
Lead Sponsor
Assiut University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Male
Target Recruitment
Not specified
Inclusion Criteria

Inclusion Criteria:<br><br> - married males<br><br> - with stable and continuous marital relationships<br><br> - diagnosed with premature ejaculation based on the International Society for Sexual<br> Medicine (ISSM-International Society for Sexual Medicine) : (a) within the 1-2<br> minutes after penetration, the ejaculation always or almost always starts; (b)in all<br> or almost all penetrations, the patient cannot delay the ejaculation; (c) PE<br> generate negative consequences on the patients, such as discomfort, frustration,<br> stress, and/or sexual intimacy avoidance<br><br> - and the patient did not take the treatment for PE in the previous 14 days<br><br>Exclusion Criteria:<br><br> - Patients were excluded if they had erectile dysfunction (measured by the<br> International Index of Erectile function-ILEF-5 questionnaire),<br><br> - inhibited male orgasm<br><br> - reduced sexual desire<br><br> - uncontrolled physical illness<br><br> - active genitourinary tract infection (confirmed by two glasses of urine according to<br> Modified Meares-Stamey technique)<br><br> - mental disorders affecting ejaculatory function such as anxiety, depression, and<br> schizophrenia, history of alcohol or drug abuse

Exclusion Criteria

Not provided

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
intravaginal ejaculation latency time
Secondary Outcome Measures
NameTimeMethod
time to ejaculation;hard erections for sufficient intercourse;satisfaction for the patient and partner
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