cervical cancer
Conditions
Interventions
Experimental group:obtaining negative vaginal margins by the guidence of frozen-section during operation
Control group:Type B/C radical hysterectomy
Sponsors
The Obstetrics and Gynecology Hospital of Fudan University
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1) Clinical diagnosis of cervical cancer (IB1-IIA2); 2) Preoperative pathological diagnosis of cervical squamous cell carcinoma, cervical adenosquamous carcinoma or cervical adenocarcinoma 3) Aged <=65 years; 4) Initial treatment; 5) Subjects volunteer to join the study, sign an informed consent form, have good compliance, and cooperate with follow-up.
Exclusion criteria
Exclusion criteria: 1) Patients' general condition is poor and severe medical complications are difficult to tolerate surgical treatment; 2) Patients who have previously received pelvic/abdominal radiotherapy or chemotherapy; 3) Patients during pregnancy; 4) Patients with other gynecological malignancies such as ovarian tumors; 5) CT, MRI or PET suggesting extracervix metastasis; 6) Those who are unable or unwilling to sign the informed consent form, and are unable or unwilling to comply with the research requirements.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Overall survival and recurrence-free survival; | — |
Contacts
Public ContactHua Keqin
The Obstetrics and Gynecology Hospital of Fudan University
Outcome results
None listed