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Study identifier: NCT07627438 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Pelvic Floor Therapies for Lifelong Premature Ejaculation

Condition: Premature Ejaculation · Lifelong Premature Ejaculation · Male Sexual Dysfunction  ·  Sponsor: Tanta University

PhaseNA
Planned participants150
Who can joinMale, 18 Years to 50 Years
Healthy volunteersNo

About this study

This randomized controlled trial will compare three pelvic floor-based treatment modalities in men with lifelong premature ejaculation: electromagnetic pelvic floor stimulation, biofeedback-assisted pelvic floor muscle training, and conventional pelvic floor muscle training. A total of 150 men aged 18 to 50 years with lifelong premature ejaculation and stopwatch-measured intravaginal ejaculatory latency time of less than 1 minute will be randomly assigned to one of the three treatment groups. The primary outcome will be the change in intravaginal ejaculatory latency time from baseline to the end of treatment at 6 weeks. Secondary outcomes will include changes in Premature Ejaculation Diagnostic Tool score, International Index of Erectile Function-5 score, patient-reported ejaculatory control, sexual satisfaction, partner satisfaction, treatment adherence, and adverse events.

This description comes directly from the study's public registry record.

Talk to the study team

Mohamed I Elmaadawy, MD  ·  +201060245430  ·  Mohamed.elmaadawy@med.tanta.edu.eg

Hany F Badawy, MD  ·  +201149525028  ·  Hanyfathy86@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Department of Urology- Tanra University HospitalsTanta, Tanta, EgyptRecruiting

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Source record: clinicaltrials.gov/study/NCT07627438