Autologous Adipose-Derived Stromal Cells Delivered Into the Corpus Cavernous in Patients With Erectile Dysfunction

AD-SVF will be collected from the patient's adipose-derived tissue (body fat). Using local
anesthesia, Liposuction will be performed to collect the adipose tissue specimen. The adipose
tissue is then transferred to the laboratory for separation of the adipose tissue derived
stem cells. In addition, peripheral blood will be collected for isolation of platelet rich
plasma, which are then combined with the ASC's for direct injection to the Corpus Cavernosum
(Penis).

Inclusion Criteria

- Males Age 18 and 80 years.

- Penile arterial insufficiency and or venous leakage (doppler) at the time o inclusion:
PSV <25 cm/sec, PSV >25 cm/sec, EDV>5cm/sec, RI<0,75.

- Up to date on all age and gender appropriate cancer screening per American Cancer
Society

Exclusion Criteria

- Severe co-morbidities like cardiac insufficiency, congestive cardiac failure (NYHA ≥
III), malignancy, infection, sepsis and bed sores.

- Life expectancy < 6 months due to concomitant illnesses.

- Exposure to any investigational drug or procedure within 1 month prior to study entry
or enrolled in a concurrent study that may confound results of this study.

- Active infectious disease. Patients known to have tested positive for HIV, HTLV, HBV,
HCV, CMV (IgM > IgG) and/or syphilis will be evaluated by an expert as to patient
eligibility based on the patient's infectious status

- Any illness which, in the Investigator's judgment, will interfere with the patient's
ability to comply with the protocol, compromise patient safety, or \ interfere with
the interpretation of the study results

- Patients on chronic immunosuppressive transplant therapy

- Systolic blood pressure (supine) ≤90 mmHg or greater than 200mmHg

- Resting heart rate > 100 bpm;

- Active clinical infection within one week of enrollment.

- Known drug or alcohol dependence or any other factors which will interfere with the
study conduct or interpretation of the results or who in the opinion of the
investigator are not suitable to participate.

- History of cancer (other than non-melanoma skin cancer or in-situ cervical cancer) in
the last five years.

- Unwilling and/or not able to give written informed consent.