Cancer Clinical Trial
Official title:
A Single Arm Multi-Center Post Approval Study of LUMA as Adjunct to Colposcopy
Verified date | May 2014 |
Source | SpectraScience |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
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.
Status | Terminated |
Enrollment | 10 |
Est. completion date | November 2010 |
Est. primary completion date | November 2010 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Documented abnormal pap test |
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Diagnostic
Country | Name | City | State |
---|---|---|---|
United States | Women's Interventional Health | Encinitas | California |
United States | U of Iowa Health Center | Iowa City | Iowa |
Lead Sponsor | Collaborator |
---|---|
SpectraScience | University of Iowa |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Relationship between HPV and the performance of the LUMA system as an adjunct to colposcopy for detection of CIN 2,3+ will be assessed. | ongoing - estimated at 3 years | No |
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