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
- Erectile Dysfunction Due to General Medical Condition
- Erectile Dysfunction Following Radical Prostatectomy
- Erectile Dysfunction Associated With Type 2 Diabetes Mellitus
- Erectile Dysfunctions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | PRP injection | 3 ML OF PRP |
| DRUG | Alprostadil 20 micrograms | 1 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.