Intrauterine Adhesion
Conditions
Interventions
experimental group:A balloon was placed three weeks after the operation to dilate the uterine cavity
control group:no bloon dilate
Sponsors
Fuxing Hospital, Capital Medical University
Eligibility
Sex/Gender
Female
Age
20 Years to 40 Years
Inclusion criteria
Inclusion criteria: 1. Understand and approve this randomized controlled trial Patients; 2. Aged 20-40 years; 3. Weight range from 50-80 kg; 4. With moderate uterine adhesion.
Exclusion criteria
Exclusion criteria: 1. a history of uterine artery embolization surgery; 2. only cervical intraoral adhesions; 3. patients with hormone replacement therapy within 3 months; 4. severe internalPatients with surgical complications; 5. pregnancy status; 6. preoperative fever or infection symptoms; 7. malignant tumors; 8. patients with a history of pelvic inflammatory disease; 9. uterine fibroids > 3cm in diameter; 10. adenomyosis; 11. patients with contraindication to anesthesia; 12. patients who do not understand or do not recognize randomized controlled trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Recurrence rate of intrauterine adhesions within 2 months after operation; | — |
Secondary
| Measure | Time frame |
|---|---|
| AFS classification; | — |
Countries
China
Contacts
Public ContactLi Tianzhao
Department of Hysteroscopic Centre, Fuxing Hospital, the Eighth Clinical Medical College, Capital Medical University, Beijing
Outcome results
None listed