Evaluating the Efficacy of Platelet-Rich-Plasma (PRP) for Erectile Dysfunction

Inclusion Criteria:

• The patient must be able willing and able to provide informed consent. Theinvestigators wil enroll males between >30 and <70 years of age who have ED based onIIEF scores (score between 16 and 25.) with patients suffering from erectiledysfunction lasting for over 6 months and not more than 5 years as per historyprovided by patient.

The patient has been in a stable relationship for over 3 months prior to enrollment with a minimum of 2 sexual attempts per month for at least one month prior to enrollment.

A1C level ≤ 7% within 1 month prior to enrollment.

Exclusion Criteria:

• Participating in another study within the past three months that may interfere withthe results or conclusions of this study, under judicial protection (prison orcustody), adult under guardianship, or patient refuses to sign the consent.

History of radical prostatectomy or extensive pelvic surgery, past radiation therapy of the pelvic region within 12 months prior to enrolment, recovering from any cancer within 12 months prior to enrollment.

Neurological disease such as Alzheimer's or Parkinson's disease which affects erectile function at the discretion of the investigator, psychiatric diagnosis or medications such as antidepressants, anxiolytic, antipsychotic that affects erectile function or any other medications at the discretion of the investigator.

Anatomical malformation of the penis, including Peyronie's disease.

A1C level > 7% within 1 month prior to enrollment or history of Insulin dependent diabetes.

The patient is taking blood thinners and has an international normalized ratio (INR) >3.

Received shockwave treatment at least 6 months before enrollment.