Menu
Recruiting NCT03466619

Penile Prosthesis in Patients With Erectile Dysfunction

No phase Interventional Erectile Dysfunction

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: inflatable penile prosthesis (IPP).
Who it may be relevant to
Registry conditions: Erectile Dysfunction. Basic parameters: 18 years — 80 years · Male.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

Erectile dysfunction (ED) is defined as the persistent inability to attain and or maintain an erection sufficient to permit satisfactory sexual performance

Detailed description

In the literature, well- designed studies evaluating safety and efficacy of inflatable penile prosthesis (IPP) is lacking. So, this series aimed at investigating this prospectively.

Interventions

  • Device inflatable penile prosthesis (IPP)
    inflatable penile prosthesis (IPP)

Primary outcome measures

  • Number of patients with improved erectile dysfunction [Time frame: 3 years]

Eligibility 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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Tanta university - faculty of medicine — Cairo

Identifiers

NCT: NCT03466619 · Khaled Hafez

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗