Erectile Dysfunction Research Study

Researchers at Ohh-Med are conducting a study on the safety and effectiveness of a new radio frequency (RF) device for the treatment of erectile dysfunction (ED) in straight adult males.

Fast Facts

Diagnosed With Erectile Dysfunction (ED) For At Least 3 Months

Straight Male

Ages 22-85

Compensation Provided

Conducted in

Bethesda, MD

Study Background

This study is evaluating a new at-home RF therapy device for men diagnosed with erectile dysfunction.

The Vertica® study is a 6-month, double-blind research study designed to assess the safety and efficacy of a non-invasive radio frequency (RF) device for treating erectile dysfunction (ED). Participants will be randomly assigned to receive either an active or sham (inactive) version of the device. The study begins with a supervised treatment session, followed by continued use of the device at home.

The device, placed between the thighs with the penis inserted into an adjustable opening, delivers RF pulses to the penis through small probes in contact with the skin. An electrode pad is also applied to the perineal area. Participants will be asked to use the device multiple times per week for several months and attempt sexual activity regularly. Monthly follow-up visits will assess safety and treatment effectiveness.

Study Background

This study is evaluating a new at-home RF therapy device for men diagnosed with erectile dysfunction.

The Vertica® study is a 6-month, double-blind research study designed to assess the safety and efficacy of a non-invasive radio frequency (RF) device for treating erectile dysfunction (ED). Participants will be randomly assigned to receive either an active or sham (inactive) version of the device. The study begins with a supervised treatment session, followed by continued use of the device at home.

The device, placed between the thighs with the penis inserted into an adjustable opening, delivers RF pulses to the penis through small probes in contact with the skin. An electrode pad is also applied to the perineal area. Participants will be asked to use the device multiple times per week for several months and attempt sexual activity regularly. Monthly follow-up visits will assess safety and treatment effectiveness.

Additional Information

The study aims to determine whether the Vertica® RF device is a safe and effective at-home treatment for men diagnosed with erectile dysfunction.

You may qualify for this study if you meet the following criteria.

Inclusion Criteria:

  • Diagnosed with erectile dysfunction (ED) for at least 3 months
  • Straight male ages 22-85
  • In a steady relationship and sexually active
  • Own a smartphone

Exclusion Criteria:

  • Experience with prolonged painful erections
  • Diagnosis of Peyronie’s Disease (curved erections)
  • History of surgery or radiotherapy involving your pelvic region
  • History of treatments for prostate conditions, including cryoablation, high-intensity focused ultrasound (HIFU), external beam radiation, seed implantation, or radical prostatectomy
  • Major neurological conditions
  • Currently dependent on any substances, such as alcohol or non-prescribed drugs
  • History of psychiatric disorders (e.g., schizophrenia, bipolar disorder)

Complete an initial email or phone screening to determine eligibility. If eligible, attend a clinical visit for diagnosis or confirmation of ED. Participate in one supervised device session simulating home use. Continue home use of the study device over 6 months.

  • Use 3x/week for 4 weeks
  • Use 2x/week for the next 4 weeks
  • Use 1–2x/week for 4 additional months

Attempt sexual activity at least once per week or 6 times/month. Attend monthly follow-up visits at 1, 2, 3, and 6 months.

You will receive $20 per completed study visit. Payments are made in two installments:

  • Half after the 3-month follow-up
  • The remainder after completing the 6-month follow-up

If you withdraw early, you’ll still be paid for completed visits.

There is no cost for you to participate in our research study.