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Trials / Enrolling By Invitation

Enrolling By InvitationNCT06768177

Platelet Rich Plasma (PRP) as Terapeutical Option in Erectil Disfunction (DE)

Status
Enrolling By Invitation
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari · Academic / Other
Sex
Male
Age
30 Years
Healthy volunteers
Not accepted

Summary

Patients are randomized into 2 groups (A and B), subsequently group A is subjected to a cycle of 6 weekly injections of 3 ml of autologous PRP while group B is subjected to 6 weekly injections of 1 ml of caverject (alprostadil) 20 mcg. After 4 (four) weeks the groups will be crossed, so group A will be subjected to 6 weekly injections of 1 ml of caverject (alprostadil) 20 mcg while group B will be subjected to a cycle of 6 weekly injections of 3 ml of autologous PRP.

Conditions

Interventions

TypeNameDescription
DRUGPRP injection3 ML OF PRP
DRUGAlprostadil 20 micrograms1 ML

Timeline

Start date
2023-04-01
Primary completion
2024-11-01
Completion
2025-11-01
First posted
2025-01-10
Last updated
2025-10-02

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT06768177. Inclusion in this directory is not an endorsement.