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Clinical Trial Summary

To demonstrate that imaging via home ultrasound can identify submucosal fibroids. The image quality and submucosal fibroid detection specificity of the home imaging has already been demonstrated; the aim of this study is to generate further data for sensitivity. This will be a single visit study, with participants scanning themselves at home with healthcare professional (HCP) supervision. Targeted population is women with previously diagnosed submucosal fibroids that have not been removed. The study will be single-blinded to the image raters.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05004870
Study type Interventional
Source Turtle Health, Inc.
Contact
Status Withdrawn
Phase N/A
Start date December 16, 2021
Completion date December 17, 2021

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