Pilot Phase for an Acute Evaluation of a Non-Implantable Electrical Continence Device

Completed · Not applicable

Conditions studied: Urinary Bladder, Overactive

In brief

The purpose of this feasibility clinical investigation is to investigate a new medical device treatment for Overactive Bladder (OAB) in women.

Key facts

Study ID

NCT04001426

Run by

FemPulse Corporation

People needed

2

Starts

2019-04-04

Expected to finish

2019-12-31

Last updated by the study team

2021-11-04

Who can join

Age: 21 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Normal healthy women ≥ 21 years old
• Using contraception if of reproductive age

You may not qualify if…

• Pregnant, recently pregnant or actively trying to conceive
• Prior hysterectomy
• Current or recent urinary tract or vaginal infection

Where it is running

• Hennepin Healthcare — Minneapolis, Minnesota, United States

Full record on ClinicalTrials.gov

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