Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
MALE
ID07627438

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

Age: 18Years - 50Years
MALE

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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

Follow-up

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

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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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