Clinical trial Recruiting at 1 site Interventional Ages 18 to 80 Men only

Implanting a penile prosthesis for erectile dysfunction

Official title: Assessment of Safety and Efficacy of Inflatable Penile Prothesis in Patients With Erectile Dysfunction

Run by Tanta University · NCT03466619 · Data updated 2026-11-12

This study tests whether an inflatable penile prosthesis can help men with erectile dysfunction who haven't found relief with other treatments feel more satisfied with their sexual performance.

Quick facts

Study typeInterventional
Ages18 Years to 80 Years
SexMen only
Enrollment100 (estimated)
SponsorTanta University
Academic / other
Locations1 site (Cairo, Elgharbia)
StatusRecruiting
StartedNovember 1, 2014
Main results expectedDecember 1, 2027
Study endsDecember 1, 2027
Registry record updatedMarch 15, 2018
Trial IDNCT03466619 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are patients with erectile dysfunction who have contraindications to or have failed medical treatments.

Probably not a fit

Patients who lack the manual dexterity or mental abilities necessary to operate the pump will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the safety and efficacy of inflatable penile prosthesis (IPP) in patients suffering from erectile dysfunction (ED) who have not responded to medical treatments. It aims to provide a prospective evaluation of the outcomes associated with this intervention. The study will enroll patients who meet specific inclusion criteria and will assess their ability to achieve satisfactory sexual performance post-implantation. The research addresses a gap in the literature regarding well-designed studies on this treatment option.

Why it matters

Potential benefit: If successful, this intervention could significantly improve sexual function and quality of life for patients with erectile dysfunction.

How similar studies have gone: While there is limited literature on the safety and efficacy of IPP, similar studies have shown promising results in improving erectile function in patients with ED.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients complaining of ED with contraindication or failure of medical treatment

Exclusion Criteria:

* Patients lacking manual dexterity or mental abilities necessary to operate the pump
* General contraindications as uncorrectable bleeding tendency

Where it's running

  • Tanta university - faculty of medicine
    Cairo, Elgharbia, Egypt
    Recruiting

Study contacts

  • Principal investigator: Khaled Mohamed Hafez Morsy Almekaty, Msc — Urology Department- Tanta University
  • Study coordinator: Sherief Abd-Elsalam, MD
  • Email: sheriefabdelsalam@yahoo.com
  • Phone: 00201095159522

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.