Active — Not RecruitingNot Applicable

Efficacy of Low-dose Percutaneous Electrical Stimulation in Patients With Erectile Dysfunction.

Spain24 participantsStarted 2023-12-01

Plain-language summary

Erectile dysfunction is known as any alteration that produces a modification in the erectile response, whether it is due to organic, psychogenic or relational causes. Peripheral percutaneous nerve stimulation is performed using a needle to stimulate the peripheral nerves in such a way as to stimulate most of the area of the structure, stimulating sensory and motor nerve endings in the deeper tissues.

Who can participate

Age range18 Years – 65 Years

SexMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: Males Ages between 18-60 years old Primarily organic cause diagnosed by Doppler: * Peak-systolic velocities (PSV). * Tele-diastolic velocity (DTV). * Resistance Index (RI) Patients with ≤ 6 months since first assessment. Initial IIEF-EF questionnaire scores: 11-25 points. (mild to moderate erectile dysfunction) Active sexual life (more than 4 attempts per month). Exclusion Criteria: Pelvic surgeries History of Peyronie's disease Penile surgeries, except circumcision or frenuloplasty Priapism Pelvic radiation Female

What they're measuring

International Index of Erectile Function (IIEF-EF)

Timeframe: 4 months

Erection Hardness Scale (EHS)

Timeframe: 4 months

Premature Ejaculation Diagnostic Tool (PEDT)

Timeframe: 4 months

Quality of Life Scale

Timeframe: 4 months

Self-Esteem And Relationship Questionnaire (Sear)

Timeframe: 4 months

Trial details

NCT IDNCT06397612

SponsorCamilo Jose Cela University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-04-15

View on ClinicalTrials.gov More Pudendal Nerve Injury trials