Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Diagnostic

Outcome Measure:

Specimen adequacy

Outcome Description:

Cytological and histological interpretation of the endocervical brush specimens will then be performed, while for the endocervical currete specimens only histological interpretation will be done. The adequacy of the specimens will be based on the quantity of endocervical cells present (< or ≥ 20 endocervical cells), the quantity of histological material (< or ≥ 3 epithelial stripes) and the quality of histological material (absence or presence of lamina propia).

Outcome Time Frame:

09/2011 - 05/2012 (1 year)

Safety Issue:

No

Authority:

Switzerland: Federal Office of Public Health

Study ID:

CER 11-029

NCT ID:

NCT01435590

Start Date:

September 2011

Completion Date:

September 2012

Related Keywords:

• Cervical Dysplasia
• Uterine Cervical Dysplasia
• Cervical Intraepithelial Neoplasia