Colli-Pee urine collection device
Diagnostic Testfirst-void urine is collected using Colli-Pee and subsequently analyzed using Anyplex™ II HPV HR Detection from Seegene.
NCT Number: NCT04864951
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.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Not applicable
Medical University of Vienna, Vienna, Austria
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
first-void urine is collected using Colli-Pee and subsequently analyzed using Anyplex™ II HPV HR Detection from Seegene.
Subjects are asked to complete a survey that includes questions about sexual orientation, hormone therapy, gender reassignment surgery, number of sexual partners, HPV vaccination, and smoking
Time frame: one year
HPV prevalence in transpeople
Sophie Pils
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05453006
Cervical Cancer, Communicable Diseases
Minneapolis, Minnesota, United States
View Trial DetailsNCT00090220
Communicable Diseases, DNA Virus Infections
View Trial DetailsNCT00828555
Bacterial Infections, Bacterial Infections and Mycoses
Burlington, North Carolina, United States
View Trial DetailsNCT00316706
Cervical Intraepithelial Neoplasia, Communicable Diseases
Bogotá, Colombia
View Trial Details