Human Papillomavirus (HPV) Self-sampling as a Test of Cure After Treatment of Cervical Intra-epithelial Neoplasia
Primary Purpose
Cervical Intra-epithelial Neoplasia Grade 1 or Worse
Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
HPV self-testing
Sponsored by
About this trial
This is an interventional prevention trial for Cervical Intra-epithelial Neoplasia Grade 1 or Worse
Eligibility Criteria
Inclusion Criteria:
- attending colposcopy clinic
- biopsy-proven CIN1+ lesion
- understands study procedures and accepts voluntarily to participate by signing the informed consent form
Exclusion Criteria:
- pregnancy
Sites / Locations
- Geneva University Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
HPV self-testing
Arm Description
Patients will perform HPV self-testing at home, prior to their follow-up visit. At the colposcopy visit, the doctor or nurse will also perform HPV testing. This procedure will be repeated at 6 and 12 months following LEEP.
Outcomes
Primary Outcome Measures
Number of patients with CIN
Number of patients with CIN after LEEP.
Secondary Outcome Measures
Full Information
NCT ID
NCT02780960
First Posted
May 13, 2016
Last Updated
January 31, 2021
Sponsor
University Hospital, Geneva
1. Study Identification
Unique Protocol Identification Number
NCT02780960
Brief Title
Human Papillomavirus (HPV) Self-sampling as a Test of Cure After Treatment of Cervical Intra-epithelial Neoplasia
Official Title
HPV Self-sampling as a Test of Cure After Treatment of Cervical Intra-epithelial Neoplasia
Study Type
Interventional
2. Study Status
Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
May 2016 (undefined)
Primary Completion Date
September 2020 (Actual)
Study Completion Date
October 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital, Geneva
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to evaluate the performance of HPV self-sampling (self-HPV) in detecting residual/recurrent disease in women treated by loop electro-surgical excision (LEEP) for CIN1+.
Detailed Description
The HPV test is an efficient method to assess the long-term risk of residual/recurrent disease in women treated for cervical intraepithelial neoplasia grade 1 or worse (CIN1+).
Women treated by LEEP for CIN1+ will be invited to participate. Follow-up visits will be performed at 6 months and 12 months after treatment and will include cytology, colposcopy when indicated and HPV testing. Two weeks before each follow-up visit at the colposcopy clinic, a home-based Self-HPV will be organized. A sample of 168 women will be included. Agreement between the two methods (Dr-HPV vs. S-HPV) will be measured using the kappa statistic (κ).
the investigators expect to find that Self-HPV may be an accurate method to predict residual and recurrent disease in women previously treated by LEEP.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cervical Intra-epithelial Neoplasia Grade 1 or Worse
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
127 (Actual)
8. Arms, Groups, and Interventions
Arm Title
HPV self-testing
Arm Type
Experimental
Arm Description
Patients will perform HPV self-testing at home, prior to their follow-up visit. At the colposcopy visit, the doctor or nurse will also perform HPV testing. This procedure will be repeated at 6 and 12 months following LEEP.
Intervention Type
Device
Intervention Name(s)
HPV self-testing
Intervention Description
Patients will perform HPV testing themselves at home.
Primary Outcome Measure Information:
Title
Number of patients with CIN
Description
Number of patients with CIN after LEEP.
Time Frame
12 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
attending colposcopy clinic
biopsy-proven CIN1+ lesion
understands study procedures and accepts voluntarily to participate by signing the informed consent form
Exclusion Criteria:
pregnancy
Facility Information:
Facility Name
Geneva University Hospital
City
Genève
ZIP/Postal Code
1205
Country
Switzerland
12. IPD Sharing Statement
Citations:
PubMed Identifier
34976630
Citation
Viviano M, Vassilakos P, Meyer-Hamme U, Grangier L, Emery SL, Malinverno MU, Petignat P. HPV self-sampling in the follow-up of women after treatment of cervical intra-epithelial neoplasia: A prospective study in a high-income country. Prev Med Rep. 2021 Sep 20;24:101564. doi: 10.1016/j.pmedr.2021.101564. eCollection 2021 Dec.
Results Reference
derived
Learn more about this trial
Human Papillomavirus (HPV) Self-sampling as a Test of Cure After Treatment of Cervical Intra-epithelial Neoplasia
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