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

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

Recruiting
21 years and older
Female
Phase N/A

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Overview

A study to evaluate the safety and effectiveness of FemPulse System

Eligibility

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.

Study details
    Overactive Bladder (OAB)

NCT07195656

FemPulse Corporation

26 February 2026

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