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More info
You can access this
clinical trial
if you have
Cervical Cancer or Cervical Intraepithelial Neoplasia
and you are
between 30 and 60
years old
The phase for this study is not defined.
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The purpose

To compare the effects of conventional cytology testing with concommitant HPV-cytology testing for the detection of high grade cervical lesions in primary cervical cancer screening in Hong Kong Hypotheses: 1. There is a significant difference in the number of CIN2+ cases detected between the cytology testing group and the cytology-HPV co-testing group at baseline. 2. Significantly more CIN2+ cases will be detected at the second round of screening among participants with normal cytology result in the control arm than those with normal cytology and negative HPV results in the intervention arm.

Provided treatments

  • Procedure: HPV-cytology co-testing

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT01058460. The sponsor of the trial is The University of Hong Kong and it is looking for 12000 volunteers for the current phase.
Official trial title:
A Randomized Controlled Trial Comparing Concomitant HPV-cytology Testing With Conventional Cytology Testing for the Detection of High Grade Cervical Intraepithelial Neoplasia in Primary Cervical Cancer Screening in Hong Kong