Cervical precancerous lesions
Conditions
Interventions
high risk group:Copy number variation
low risk group:Copy number variation
Sponsors
Shanghai General Hospital
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1.Han nationality, female, aged 18 or above with a history of sexual life; 2.Subjects who have clinical HPV and TCT test; 3.Subjects with remaining clinical samples after HPV test;
Exclusion criteria
Exclusion criteria: 1.Subjects with acute inflammation of the reproductive tract; 2.Subjects with sexual life history, vaginal lavage or local drug administration within 72 hours; 3.Subjects with history of pelvic chemoradiotherapy, cervical surgery or total hysterectomy; 4.Subjects who have or had other cancers (except cervical cancer); 5.Subjects with autoimmune diseases and/or taking immunosuppressants; 6.Subjects with incomplete information, including: HPV test results, TCT test results; age, gravidity, parity and other clinical information; 7.Special populations (those with psychosis, cognitive dysfunction, and pregnant or lactating women).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| copy number variations; | — |
Secondary
| Measure | Time frame |
|---|---|
| thinprep cytologic test;human papillomavirus detection and genotyping; | — |
Countries
China
Contacts
Public ContactDong Hui
Shanghai General Hospital
Outcome results
None listed