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Penile Prosthesis in Patients With Erectile Dysfunction

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03466619
Enrollment
100
Registered
2018-03-15
Start date
2014-11-01
Completion date
2027-12-01
Last updated
2018-03-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Erectile Dysfunction

Brief summary

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

DEVICEinflatable penile prosthesis (IPP)

inflatable penile prosthesis (IPP)

Sponsors

Tanta University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

inflatable penile prosthesis (IPP)

Eligibility

Sex/Gender
MALE
Age
18 Years to 80 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Number of patients with improved erectile dysfunction3 yearsThe number of patients with improved erectile dysfunction

Countries

Egypt

Contacts

Primary ContactSherief Abd-Elsalam, MD
sheriefabdelsalam@yahoo.com00201095159522

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026