The purpose of this study is to evaluate the safety and efficacy of adipose derived cells for
the treatment of erectile dysfunction symptoms.
Device: Tissue Genesis Cell Isolation System
We will connect you to the doctor responsible for this trial and help you get more information.
Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT01601353
Ages eligible for Study
40 Years to 70 Years
Genders eligible for Study
Accepts Healthy Volunteers
Men aged 40 - 70
Willing and able to provide written informed consent
Chronic, organic erectile dysfunction (ED), duration at least 0.5 years, with baseline International Index of Erectile Function - Erectile Function (IIEF-EF) score of < 26
Willing to complete questionnaires
Involved in a monogamous, heterosexual relationship for at least 3 months with both partners motivated to have or attempt sexual intercourse at least 4 times per month beginning two weeks after study treatment (subject reported)
Not interested or able to use oral PDE-5 inhibitor (PDE-5i) drug therapy, and willing to forgo these treatments for the first 6-month period following study treatment (in addition may include a minimum 4-week washout since last PDE-5i use prior to completion of the baseline erectile function assessments and study treatment)
Willing to limit alcohol intake and eliminate use of recreational drugs for sexual encounters
Willing to undergo a minor surgical procedure and injection
Abdominal area amenable to liposuction of at least 60-120 cc of adipose tissue based on Investigator examination
Mentally competent and able to understand all study requirements (based on investigator assessment)
Willing to be available for all baseline, treatment and follow-up examinations required by protocol
Willing to forego participation in any other study throughout the duration of this study unless receiving prior approval by Sponsor.
Evidence of prostate cancer which requires additional radiotherapy or other adjuvant therapy
Previous pelvic or abdominal radiation therapy
Previous, concomitant or scheduled use of anti-androgen therapy
Untreated hypogonadism or low serum total testosterone (< 200 ng/dL)
Clinically evident penile anatomical deformities (e.g., Peyronie's disease) or history of priapism
Skin irritation, infection, wound, sore or disruption in the immediate areas of skin entry for abdominal liposuction or penile injection (including abdominal trauma and abdominal skin cancer (basal cell carcinoma, squamous cell carcinoma, and melanoma))
Use of any non-study treatment for erectile dysfunction within 4 weeks of study treatment and a lack of willingness to continue through 6 months after study treatment
Any previous penile implant or penile vascular surgery
Current or previous malignancy other than localized prostate cancer or nonabdominal, non-melanoma skin cancer (successfully treated or treatable by curative excision or other local curative therapy- abdominal skin cancer is exclusionary as indicated in criteria 6)
Uncontrolled hypertension or hypotension (systolic blood pressure > 170 or < 90 mm Hg, and diastolic blood pressure > 100 or < 50 mm Hg)
Reported unstable cardiovascular disease (e.g., unstable angina, myocardial infarction within past 6 months, cardiac failure or life-threatening arrhythmia, congestive heart failure) or symptomatic postural hypotension within 6 months before screening
Hemoglobin A1c > 8% within 8 weeks prior to study treatment
Current urinary tract or bladder infection
Drug, alcohol, or substance abuse reported within the last three years (subject reported)
Subject's sexual partner is < 18 years of age, nursing, or known to be pregnant at screening, or wishes to become pregnant during the study period, or has any gynecologic problems, major medical conditions, or other factors that would limit participation in sexual intercourse to less than 4 times per month (subject reported)
Weight less than 154 lbs/ 70 kg, or BMI ≥ 30
Unable to limit or avoid nonsteroidal anti-inflammatory drugs(NSAIDs) for 15 days prior to treatment (subject reported)
Bleeding or clotting disorder, use of anticoagulant therapy, or history of easy or excessive bruising
Lab values for Complete Blood Count(CBC), Prothrombin Time(PT)/Partial Thromboplastin Time(PTT)/International Normalized Ration(INR), liver function and creatinine falling outside the normal lab values (see section 5.3 for further detail)
Systemic autoimmune disorder
Significant active systemic or localized infection
Receiving immunosuppressant medications
All locations for NCT01601353
United States (2)
San Diego Sexual Medicine
San Diego, California, United States, 92120
Baylor College of Medicine
Houston, Texas, United States, 77030
View full eligibility
Tris trial is registered with FDA with number: NCT01601353. The sponsor of the trial is Tissue Genesis, LLC and it is looking for 30 volunteers for the current phase.
Official trial title: Evaluate the Use of Liposuction and Cell Separation Devices for Autologous Fat (Adipose) Derived Cells to Treat the Symptoms of Erectile Dysfunction
Thank you for applying!
We'll contact you soon with more information.
FindMeCure is constantly improving its search. Take part in it and help millions by filling our patients' survey!