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ENROLLING BY INVITATION
NCT06768177
NA

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

Sponsor: Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari

View on ClinicalTrials.gov

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.

Key Details

Gender

MALE

Age Range

30 Years - Any

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2023-04-01

Completion Date

2025-11-01

Last Updated

2025-10-02

Healthy Volunteers

No

Interventions

DRUG

PRP injection

3 ML OF PRP

DRUG

Alprostadil 20 micrograms

1 ML

Locations (1)

Policlinico di Bari - Azienda Ospedaliero Universitaria Consorziale Policlinico

Bari, Italy