HPV-test, Cervical Cancer and Follow-up
- Conditions
- Human Papilloma VirusUterine Cervical NeoplasmsRecurrence
- Interventions
- Procedure: Human Papilloma Virus test from the vaginal vault
- Registration Number
- NCT02096016
- Lead Sponsor
- University of Aarhus
- Brief Summary
The investigators have planned this project to evaluate the follow-up program after surgery due to cervical cancer and to explore the possibilities for different tests of Human Papilloma Virus (HPV) in contributing to the customization of the follow-up program.
Purpose:
The investigators effort is to provide the background for an evidence-based update of the follow-up program after surgery due to cervical cancer with the purpose of early diagnosis of recurrence affecting quality of life for as few women as possible.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- Female
- Target Recruitment
- 50
Inclusion Criteria
- Surgery. FIGO stage IA-IB. > 18 years
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Exclusion Criteria
- Ajuvant oncologic treatment
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Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Human Papilloma Virus test Human Papilloma Virus test from the vaginal vault Patients treated with surgery alone for uterine cervical neoplasms attending surveillance at Dept. of Obstetrics and Gynecology, Oncogynecological unit, Aarhus University Hospital from 01.01.14 From 01.01.15 patients will be recruited from Oncogynecologic units at Aalborg University Hospital and Rigshospitalet. Recruitment of patients from these institutions has not been successful and has been closed. It is expected due to political decisions that the cervical cancer patients from the uptake area of Aalborg University Hospital will be treated at Aarhus University Hospital and they will then be eligible for the study
- Primary Outcome Measures
Name Time Method Prevalence of HPV Genotypes in Vagina (Type 16, 18 and Other) 2 years
- Secondary Outcome Measures
Name Time Method HPV Clearance From Vagina in Between the Two Planned Follow-up Visits. 2 years
Trial Locations
- Locations (1)
Aarhus University Hospital
🇩🇰Aarhus, Denmark