Study of LUMA Cervical Imaging System as Adjunct to Colposcopy
Stopped early · Phase 4
Conditions studied: Dysplasia, Cancer
In brief
This is a post-approval, multi-center, single-arm study (n=950) designed to address the relationship of the LUMA device performance to patient age, patient human papillomavirus (HPV) status and colposcopist experience.
Key facts
- Study ID
- NCT00358111
- Run by
- SpectraScience
- People needed
- 10
- Starts
- 2006-07-01
- Expected to finish
- 2010-11-01
- Last updated by the study team
- 2014-05-13
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Documented abnormal pap test
Where it is running
- Women's Interventional Health — Encinitas, California, United States
- U of Iowa Health Center — Iowa City, Iowa, United States
Full record on ClinicalTrials.gov
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