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Evaluation of a Non-Implanted Electrical Stimulation Device for Overactive Bladder (OAB)

FemPulse Corporation · with Moxie Clinical · NCT07195656

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 21+ · Women only
Healthy volunteers
Not accepted (a condition is required)
Study type
Interventional · Not applicable
Target enrollment
151
US sites recruiting
12
Study start
September 30, 2025
Record last updated
July 13, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

A study to evaluate the safety and effectiveness of FemPulse System

Being studied: Device Group; Medication Group

Conditions: Overactive Bladder (OAB)

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Key Inclusion Criteria

  • Females, defined as a person with a uterus and cervix, ≥21 years old, with a diagnosis of OAB and symptoms for more than 6 months, as confirmed by a physician. OAB is defined by urinary urgency, usually with urinary frequency and nocturia, with or without urgency urinary incontinence with symptoms
  • Willing and able to comply with study required procedures and visits (e.g., maintaining consistent medication use, fluid intake, diary completion).

Key Exclusion Criteria

  • Systemic condition or disease that may interfere with study participation (e.g., current systemic infection, uncontrolled autoimmune disease, uncontrolled immunodeficiency disease, history of myocardial infarction, etc.) as determined by study investigator.
  • Not an appropriate study candidate as determined by investigator.

Recruiting US locations

  • Cedars Sinai

    Beverly Hills, CA 90211

    Site contact: Arman Jordan · 310-248-6716 · arman.jordan@cshs.org

  • UCLA

    Los Angeles, CA 90095

    Site contact: Katie Levitt · (310) 794 - 6786 · KLevitt@mednet.ucla.edu

  • UC Irvine

    Orange, CA 92868

    Site contact: Bryan Robles · 714-509-6130

  • Stanford

    Palo Alto, CA 94304

    Site contact: Kathryn Batham · 650-724-7826

  • USCD

    San Diego, CA 92037

    Site contact: Melissa Saurez · 858-249-4447

  • Holy Cross Medical Group - Women's Center

    Fort Lauderdale, FL 33334

    Site contact: Judie Corbett · 954-542-4841

  • Comprehensive Urologic

    Barrington, IL 60010

    Site contact: Sunny Sian · 847-852-1777

  • Chesapeake Urology

    Owings Mills, MD 21117

    Site contact: Seema Shahi · 410-616-8431

  • Adult & Pediatric Urology

    Omaha, NE 68114

    Site contact: Peyton Schneider · 402-399-7898

  • Atrium Health

    Charlotte, NC 28204

    Site contact: Robbin Clark · 704-355-7466

  • Southern Urogynecology

    West Columbia, SC 29169

    Site contact: Tina McCready · 803-457-7000

  • Sanford Health

    Sioux Falls, SD 57105

    Site contact: Jennifer Pratt · 605-328-1391

Study contacts (from the official record)

  • Monica Unger · 7275123718 · monica.unger@moxieclinical.com
Evaluation of a Non-Implanted Electrical Stimulation Device for… (NCT07195656) | Bored Studies