Trials / Completed
CompletedNCT06885099
Ease of Use Study of the FemPulse System
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 11 (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
Detailed description
The objective of the study is to demonstrate that the FemPulse System can be used as indicated in the Patient and Clinician 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
- 2025-02-11
- Primary completion
- 2025-07-31
- Completion
- 2025-07-31
- First posted
- 2025-03-20
- Last updated
- 2026-02-06
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06885099. Inclusion in this directory is not an endorsement.