Physician's Comfort Level and Satisfaction Study With The e2TM Collector Compared to the Spatula/CytoBrush Technique

Clinical Study Assessing Physician's Comfort Level and Satisfaction When Using The e2TM Cervical Cell Collector Compared to the Standard Spatula/CytoBrush Technique

Status

Terminated

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00496314

Enrollment

Registered

2007-07-04

Start date

2007-05-31

Completion date

2008-01-31

Last updated

2008-06-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical Cell Collection

Brief summary

A study which assesses the physician's comfort level and satisfaction when using the e2TM Collector compared to the Spatula/SytoBrush technique.

Interventions

DEVICEe2TM Cervical Cell Collector

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Healthy volunteers

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.)

Design outcomes

Primary

Measure	Time frame
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.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026