Actively Recruiting
Electromagnetic Pelvic Floor Stimulation Versus Biofeedback-Assisted and Conventional Pelvic Floor Muscle Training in Men With Lifelong Premature Ejaculation: A Randomized Controlled Trial
Led by Tanta University · Updated on 2026-06-04
150
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating three pelvic floor-based treatments for men with lifelong premature ejaculation, a common male sexual condition that can affect quality of life and relationships. The trial compares electromagnetic pelvic floor stimulation, biofeedback-assisted pelvic floor muscle training, and conventional pelvic floor muscle training. Men aged 18 to 50 years with an intravaginal ejaculatory latency time of less than 1 minute will participate. The study is randomized and controlled to determine which treatment may improve ejaculatory control. Participants will be randomly assigned to one of three groups: electromagnetic pelvic floor stimulation delivered non-invasively over 6 weeks, supervised biofeedback-assisted pelvic floor muscle training over 6 weeks to enhance muscle awareness and coordination, or conventional pelvic floor muscle training over 6 weeks following institutional protocols. Each treatment aims to improve pelvic floor muscle function and ejaculatory control. During the study, men will undergo baseline assessments including medical and sexual history, physical exams, stopwatch measurements of ejaculatory latency time, and questionnaires about sexual function and satisfaction. Outcomes will be measured at baseline, after 6 weeks of treatment, and at 3 months follow-up. Researchers will monitor treatment adherence and any adverse events throughout the trial, focusing on changes in ejaculatory latency time and patient-reported outcomes.
CONDITIONS
Brief Title
Pelvic Floor Therapies for Lifelong Premature Ejaculation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Men aged 18 to 50 years
- Diagnosis of lifelong premature ejaculation
- Intravaginal ejaculatory latency time less than 1 minute
- Ability and willingness to comply with the treatment protocol and follow-up visits
- Written informed consent
You will not qualify if you...
- Erectile dysfunction
- Neurological disease
- Previous pelvic surgery
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 6 weeks
Participants receive one of three pelvic floor therapies—electromagnetic pelvic floor stimulation, biofeedback-assisted pelvic floor muscle training, or conventional pelvic floor muscle training—to improve ejaculatory control.
Weekly visits for up to 6 weeks
Duration - 3 months
Participants are assessed to evaluate treatment effects and changes in ejaculatory latency and sexual satisfaction after the treatment period.
1 follow-up visit (in-person)
Trial Site Locations
Total: 1 location
1
Department of Urology- Tanra University Hospitals
Tanta, Tanta, Egypt
Actively Recruiting
Research Team
M
Mohamed I Elmaadawy, MD
H
Hany F Badawy, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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