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Clinical Trial Summary

In this study, Human Papilloma Virus (HPV) prevalence will be determined once in the urine of 200 trans people. In addition, subjects will be asked to complete a questionnaire about their sexual orientation, which is adapted from the largest published study.

Clinical Trial Description

All transpeople who visit the outpatient clinic are asked to participate in the study. After being informed and signing the Informed Consent Form, the subjects are asked to give first-void urine and fill out the survey. The urine samples are sent pseudonymously to the University of Ljubljana for analysis. The subjects will be informed about their results within 3 weeks.If the result is positive, the subjects will be offered voluntary further care in our HPV outpatient clinic. However, this will take place outside the study. The data collected there can be used for further analyses. ;

Study Design

Related Conditions & MeSH terms

NCT number NCT04864951
Study type Interventional
Source Medical University of Vienna
Contact Sophie Pils, MD
Phone 004314040029150
Email [email protected]
Status Not yet recruiting
Phase N/A
Start date May 2021
Completion date May 2022

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