Physician's Comfort Level and Satisfaction Study With The e2TM Collector Compared to the Spatula/CytoBrush Technique
Terminated
- Conditions
- Cervical Cell Collection
- Registration Number
- NCT00496314
- Lead Sponsor
- CytoCore, Inc.
- Brief Summary
A study which assesses the physician's comfort level and satisfaction when using the e2TM Collector compared to the Spatula/SytoBrush technique.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
- Every Physician who will participate in the two CytoCore prospective studies assessing the safety and efficacy of the e2TM Collector
- Each physician will have used the Collector 15 - 25 times
- Each physician will have signed the Consent form prior to using the Collector for the first time.
Exclusion Criteria
- None (commensurate with the above inclusion conditions.)
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Physician comfort level and satisfaction when using the e2TM Collector compared to the standard spatula/cytobrush. Each physician will be surveyed after first and last use of the e2TM collector as well as three more times spaced at near regular intervals in between.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
University Hospital CASE Medical Center
🇺🇸Cleveland, Ohio, United States