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More info
You can access this
clinical trial
if you have
Human Papillomavirus Infection
and you are
over 20
years old
-
The phase for this study is not defined.
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The purpose

Human papillomavirus (HPV) assays are likely to be used in cervical cancer screening. Our objective is to simplify the method of collection of female genital tract specimens by determining if vaginal dry swabs are as accurate as the standard transport medium for HPV diagnosis.

Provided treatments

  • Other: Compare different self-obtained specimen for HPV identification
  • Other: Compare different self-obtained specimen for HPV identification

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: NCT01316120. The sponsor of the trial is University Hospital, Geneva and it is looking for 120 volunteers for the current phase.
Official trial title:
Randomized Comparison of Vaginal Self Sampling for Human Papillomavirus (HPV) Testing by Standard Versus Dry Vaginal Swabs