POMx In the Treatment of Erectile Dysfunction

Completed · Phase 2 · Has a placebo group

Conditions studied: Erectile Dysfunction

In brief

POMx can be used as a treatment for erectile dysfunction.

Key facts

Study ID

NCT01220206

Run by

POM Wonderful LLC

People needed

120

Starts

2011-08-01

Expected to finish

2012-10-01

Last updated by the study team

2012-10-05

Who can join

Age: 21 and older, up to 70. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Male 21 to 70 years old
• Erectile Function domain score of 10-19 on the International Index of Erectile Function (IIEF)
• In a stable, monogamous relationship with a consenting female partner and willing to attempt vaginal sexual intercourse on at least one occasion per week on average during each study period
• History of ED (clinically defined as the inability to attain and maintain an erection of the penis sufficient to permit satisfactory sexual intercourse) of at least 3 months duration
• Treated previously with a PDE-5 inhibitor with a satisfactory response, as defined by the patient.
• Signed informed consent

You may not qualify if…

• The presence of any of the following excludes a subject from study enrollment: ED caused by untreated endocrine disease, i.e., hypopituitarism, hypothyroidism, hypogonadism
• A diagnosis of situational psychogenic ED
• Significant penile pathology, including but not limited to curvature, fibrosis, sexually transmitted disease, and penile implant
• Clinically significant hepatic, renal, neurological disease, diabetes mellitus, spinal cord injury, significant coronary heart disease, significant neurological disease or hepatitis B and/or C
• History of prostate cancer or prostate surgery other than a transurethral resection of the prostate
• History of alcoholism within the previous 2 years
• Current consumer of three or more units of alcohol per day (1 unit is equivalent to 1 glass of wine, 1 pint of beer, or 1 shot of hard liquor)
• Taking ED therapy (prescription medications, over-the-counter medications, herbal preparations or medical devices) after the screening visit
• Participation in another study with an investigational drug or device during the 30 days prior to study entry
• Has a condition interfering with his ability to provide informed consent or comply with study instructions

Where it is running

• Medical Affiliated Research Center — Huntsville, Alabama, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.