Implanting a penile prosthesis for erectile dysfunction
Assessment of Safety and Efficacy of Inflatable Penile Prothesis in Patients With Erectile Dysfunction
NA · Tanta University · NCT03466619
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
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | Male |
| Sponsor | Tanta University (other) |
| Locations | 1 site (Cairo, Elgharbia) |
| Trial ID | NCT03466619 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this study are patients with erectile dysfunction who have contraindications to or have failed medical treatments.
Not a fit: Patients who lack the manual dexterity or mental abilities necessary to operate the pump will not benefit from this study.
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 performed: 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.
Eligibility criteria
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 this trial is running
Cairo, Elgharbia
- 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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Erectile Dysfunction