Clinical Trial for the Use of a Novel Cell Collector Device to Retrieve Cells From the Uterine Cervix

University Hospitals (UH)

Status: Completed

Conditions: Uterine Cervical Cancer; Uterine Cervical Neoplasia; Uterine Cervical Intraepithelial Neoplasia; Uterine Cervical Dysplasia

Study type: Observational

Funder types: Other

Identifiers

NCT00266084

02-00-16

Details and patient eligibility

About

This study tested the safety and performance of a new cell collector device and compared the results to those obtained with the current existing device that are being used routinely

Full description

This study tested the feasibility, safety and efficacy of the new e2TM Collector, and compared its performance with the standard method for obtaining cervical cells for Pap test of endocervical cytobrush and Ayer's Spatula

Sex: Female

Ages: 14+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

Women ages >14 being followed for a previous abnormal Pap All patients will have signed an Informed Consent form prior to being enrolled in this study

Exclusion criteria

Patients who have had a hysterectomy