Expired Study
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Albuquerque, New Mexico 87106


Purpose:

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


Study summary:

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.


Criteria:

Inclusion Criteria: - Subjects must meet the approved Instructions for Use for the Symphion® bipolar hysteroscopic tissue resection system - Confirmation hysteroscopic evaluation to access appropriate pathology type and size meets the Protocol guidelines for inclusion - Subject has signed written Informed Consent Exclusion Criteria: - Subjects who are pregnant - Subjects who have an active genital tract infection (as assessed by the physician) - Subjects who have cervical malignancies - Subjects who have previously been diagnosed with endometrial cancer - Subjects who have Type 2 intracavitary myomas - Type 0 or 1 intracavitary myoma greater than 3.0 cm


NCT ID:

NCT02520414


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Albuquerque, New Mexico 87106
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 20, 2017

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