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EVANESCE II Clinical Study

EVANESCE II Clinical Study

Now Enrolling Women with Symptoms of Overactive Bladder (OAB)

Southern Urogynecology Wellness & Aesthetics is currently enrolling participants for the EVANESCE II Clinical Study.

The purpose of this study is to evaluate the FemPulse System, a non-implanted vaginal electrical stimulation device intended to treat women with symptoms of Overactive Bladder (OAB).

The FemPulse System includes a small, soft vaginal ring that provides mild electrical stimulation to surrounding tissue. The device is controlled by a handheld remote control and recharged using a small charger. The study is designed to evaluate the safety and effectiveness of this investigational system.

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Basic Eligibility Requirements

You may qualify for the study if you:

  • Are female 21 years of age or older
  • Experience symptoms of Overactive Bladder (OAB)
  • Are not currently pregnant
  • Are able to attend required study visits
  • Are willing to complete study-related diary entries

Participants may receive study-related care and compensation for time and travel.

If you meet the needs mentioned and you would like to learn more, please call our office at 803-457-7000 or email tmcgready@southurogyn.com

Please note that only our staff can determine if a candidate meets full eligibility requirements.

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