Genital HPV infection HPV infection of the cervix and vulva
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Female sex; - Age >= 18 years at start of the study; - Eligible for renal transplantation; - Operation at the Radboud University Nijmegen Medical Centre
Exclusion criteria
Exclusion criteria: - Patient not willing to sign and/or return the informed consent form; - Patient refusing additional treatment in case of abnormal findings at the first visit; - Patient being pregnant, or within a period of 3 months after delivery; - Patient being within a period of 3 months after miscarriage.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main study parameter is the prevalence of hr-HPV infections before and after renal transplantation. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints are the incidence of HPV infections before and after renal transplantation and the genotype of the HPV infections per time point, and the findings of gynaecological examination before transplantation in relation with the hrHPV status, viral load of a hrHPV infection in time, quality of life before and after transplantation and the correlation of the quality of life with the incidence/prevalence of genital HPV infection/genital (pre)malignant lesions | — |
Countries
Netherlands