Symphion® System In-Office Study

Uterine Leiomyomas Clinical Trial

Official title:
A Pilot Study to Assess the Feasibility of the Symphion® Bipolar Hysteroscopic Tissue Resection System in an Office Environment

Status Completed

Clinical Trial Summary

The purpose of this study is to determine the safety and feasibility of using the Symphion system in an office setting.

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02520414
Study type	Interventional
Source	Minerva Surgical, Inc.
Contact
Status	Completed
Phase	N/A
Start date	November 2014
Completion date	April 2015

View Details

See also
Status	Clinical Trial	Phase
Recruiting	`NCT02293447` - Intra-arterial Lidocaine for Pain Control Post Uterine Fibroid Embolization	Phase 4
Completed	`NCT02829333` - The Effect of Anesthetic Technique on VEGF-C and PGE2	N/A
Completed	`NCT00340288` - Fibroid Growth Study
Completed	`NCT01141062` - Therapeutic MRI Guided High Intensity Focused Ultrasound Ablation of Uterine Fibroids	Phase 3
Completed	`NCT01064960` - Therapeutic MRI-HIFU Ablation of Uterine Fibroids in a 3T MRI Scanner	Phase 3
Completed	`NCT00295217` - MR Guided Focused Ultrasound Surgery in the Treatment of Uterine Fibroids: Software V4.2 Validation	Phase 3
Completed	`NCT01936493` - Biologic Predictors of Leiomyoma Treatment Outcomes	N/A