Trials / Completed
CompletedNCT06347380
Usability Study of the FemPulse System
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 5 (actual)
- Sponsor
- FemPulse Corporation · Industry
- Sex
- Female
- Age
- 21 Years
- Healthy volunteers
- Not accepted
Summary
The objective of the study is to demonstrate that the FemPulse System can be used as indicated in the Instructions for Use (IFU), as applicable.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | FemPulse System | Subjects to receive the FemPulse System consisting of a non-implanted, vaginal electrical stimulation device (Ring) and other patient accessories. |
Timeline
- Start date
- 2024-09-11
- Primary completion
- 2025-07-31
- Completion
- 2025-07-31
- First posted
- 2024-04-04
- Last updated
- 2026-02-06
Locations
2 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06347380. Inclusion in this directory is not an endorsement.