Evaluating the Visual Appearance of Cervical Lesions in Relation its Histological Diagnosis, Human Papillomavirus Genotype and Other Viral Parameters: A Prospective Cohort Study.
Recruiting
- Conditions
- Cervical Intraepithelial Neoplasia, Cervical Lesion, Human PapillomavirusCervicale Intraepitheliale Neoplasie, Humaan Papillomavirus
- Registration Number
- NL-OMON21093
- Lead Sponsor
- Performers:- DDL Diagnostic Laboratory, Rijswijk, The Netherlands- Reinier de Graaf Groep, Delft, The Netherlands- Hospital Clinic, Barcelona, Spain
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 600
Inclusion Criteria
1. An abnormal cytological test result;
2. 18 years of age or older;
Exclusion Criteria
1. History of surgery on the cervix;
2. Previous pelvic radiotherapy;
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method In the follow-up period of the study, the endpoint will be the histologically confirmed recurrence of a<br>high-grade cervical lesion, defined as CIN 2 or 3, AIS or worse, or after the colposcopic examination<br>24 months after the first visit has been performed.
- Secondary Outcome Measures
Name Time Method