Cervical cancer, high-grade precancerous lesions, low-grade precancerous lesions
Conditions
Interventions
The group of low-grade precancerous lesions:None
The normal control group:None
The group of high-grade precancerous lesions:None
The cervical cancer group:None
Sponsors
International Peace Maternity and Child Health Hospital of China Welfare Institute
Eligibility
Sex/Gender
Female
Age
25 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Women aged 25 years or above, with a history of sexual activity and who are not pregnant. 2. The cervix is intact before the diagnosis and surgery. 3. No previous history of malignant tumor. 4. Sufficient tissue samples that meet the standards can be collected to complete the detection. 5. Be informed and consent;
Exclusion criteria
Exclusion criteria: 1. The medical record information is incomplete (including information such as gender, age, clinical pathological diagnosis results, and other demographic data, etc.). 2. Before this screening, diagnosis and treatment, there is a history of high-grade cervical lesions (CIN2, CIN3, cervical cancer) and a history of treatments such as surgery. 3. Those who withdraw from this study midway before reaching the research endpoint. 4. Subjects whose sample size does not meet the requirements;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Whole genome sequencing; | — |
Countries
China
Contacts
Public ContactDan Wu
International Peace Maternity and Child Health Hospital of China Welfare Institute
Outcome results
None listed