Trials / Completed
CompletedNCT02520414
Symphion® System In-Office Study
A Pilot Study to Assess the Feasibility of the Symphion® Bipolar Hysteroscopic Tissue Resection System in an Office Environment
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 10 (actual)
- Sponsor
- Minerva Surgical, Inc. · Industry
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine the safety and feasibility of using the Symphion system in an office setting.
Detailed description
The purpose is to determine the safety and feasibility of using an intrauterine tissue resection system in the office setting, as well as to expand the national discussion regarding in-office hysteroscopic procedures as it relates to the highest standards of care and cost containment.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Symphion® Bipolar Hysteroscopic Tissue Resection System |
Timeline
- Start date
- 2014-11-01
- Primary completion
- 2015-03-01
- Completion
- 2015-04-01
- First posted
- 2015-08-11
- Last updated
- 2021-03-26
- Results posted
- 2017-06-07
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02520414. Inclusion in this directory is not an endorsement.