An observational study in Uterine Cervical Dysplasia, Uterine Cervical Intraepithelial Neoplasia and Uterine Cervical Neoplasia, sponsored by University Hospitals Cleveland Medical Center. Completed. Open to female participants aged 14 Years and older. Per ClinicalTrials.gov, last updated 2016-05-11.
Sponsored by University Hospitals Cleveland Medical Center · Observational
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
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
1,881 studies on the registry are indexed under Uterine Cervical Neoplasms; 567 are open to participants now.
This study's enrollment of 85 is below the median of 220 across 419 observational studies indexed under Uterine Cervical Neoplasms.
Browse Uterine Cervical Neoplasms studies →University Hospitals Cleveland Medical Center is the lead sponsor of 283 studies on the registry; 42 are open to participants now.
Of its 32 completed or terminated interventional studies of FDA-regulated products, 29 (91%) have results posted.
Counted across the registry records on this site, refreshed daily.
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
No study locations are listed for this record.
This study is completed, as verified in Nov 2001. You cannot join it, but the record below documents what was studied.
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University Hospitals Cleveland Medical Center