Cervical stenosis
Conditions
Interventions
Group A:Cervical dilation group:Group A underwent cervical dilation three times at 3-4 weeks, 5-6 weeks, and 7-8 weeks after LEEP surgery. The specifications of the metal Hegar cervical dilation rods
Group B: Clinical observation group:No
Sponsors
International Peace Maternity and Child Healthcare Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
Eligibility
Sex/Gender
Female
Age
40 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Menopausal patients who have stopped menstruation for 1+ years[9] after LEEP; 2. Patients with cervix (including patients after subtotal hysterectomy). 3. Those who undergo colposcopy and LEEP surgery in our hospital and have complete colposcopy data and surgical records. 4. LEEP patients who have a clear external cervical opening under colposcopy before LEEP and can undergo cervical curettage.
Exclusion criteria
Exclusion criteria: 1. Patients who experience significant bleeding from the cervical wound after LEEP surgery and have secondary cervical wound hemostasis; 2. Patients with cervical malignant tumors; 3. Patients who have already experienced cervical stenosis before LEEP surgery; 4. Medications (oral or injectable) causing drug-induced amenorrhea.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cervical stenosis rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Cervical stenosis rate; | — |
Countries
China
Contacts
Public ContactDan Wu
International Peace Maternity and Child Healthcare Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
Outcome results
None listed