Mail-in HPV Screening Program in NJ
NCT07575217
Cervical Cancer Screening
View Trial DetailsNCT Number: NCT07545525
Patients indicated for subtotal hysterectomy will be tested for High risk HPV and if the result is positive will undergo expert colposcopy and conisation if not indicated otherwise at the time of subtotal hysterectomy
Trial opening soon.
Get Notified18 year and older
Female
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 3 years
Prevalence of HPV positivity in the tested cohort (patients indicated for subtotal hysterectomy).
Prevalence of HPV (other than HPV 16 and 18) positivity in the tested cohort (patients indicated for subtotal hysterectomy).
Prevalence of abnormal oncological cytology result and correlation to HPV result in the tested cohort (patients indicated for subtotal hysterectomy).
Prevalence of cervical intraepithelial leasions in patients who underwent cone biopsy with the subtotal hysterectomy.
Prevalence of high grade cervical intraepithelial leasions in patients who underwent cone biopsy with the subtotal hysterectomy.
Rate of HPV negativity 6 months after cone biopsy.
Contact information is provided by the study sponsor or research team.
General University Hospital, Prague
Other
HPV Testing as a Prevention of Cervical Dysplasia and Cervical Cancer Before Planned Subtotal Hysterectomy
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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.
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