Symphion® System In-Office Study
NCT02520414 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10
Last updated 2021-03-26
Summary
The purpose of this study is to determine the safety and feasibility of using the Symphion system in an office setting.
Conditions
- Uterine Leiomyomas
- Endometrial Polyps
Interventions
- DEVICE
-
Symphion® Bipolar Hysteroscopic Tissue Resection System
Sponsors & Collaborators
-
Minerva Surgical, Inc.
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2014-11-30
- Primary Completion
- 2015-03-31
- Completion
- 2015-04-30
Countries
- United States
Study Locations
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