Imaging the Uterine Cervix - UltraSightHD™

Completed

Conditions studied: Uterine Cervical Neoplasms

In brief

The purpose of this study is to investigate the performance ability of the UltraSightHD™. The instrument will be assessed on characteristics such as focus quality, ability to image the entire cervix, and illumination. The information gathered from this study will provide data that will be used to determine which settings provide the best imaging outcome for the cervix for a simple screening instrument. Further, this information will serve as the foundation in the development of more advanced follow-on imaging devices. The primary objectives of this study are to: * Determine if the light source provides sufficient illumination of the cervix. * Assess focus and overall image quality. * Assess the functionality and ergonomics of the instrument's design.

Key facts

Study ID

NCT01090635

Run by

STI-Medical Systems

People needed

12

Starts

2010-03-01

Expected to finish

2011-02-01

Last updated by the study team

2011-02-04

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Healthy Female
• 18 years old or older
• Not pregnant
• Ability to give consent

You may not qualify if…

• Male
• Less than 18 years old
• Pregnant or suspected pregnancy

Where it is running

• Dr. Nathan Fujita — Honolulu, Hawaii, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.