intrauterine adhesion
Conditions
Interventions
Experimental group:Hysteroscopic adhesion separation+uterine balloon placement+HRT+ Qushi Yangmo prescription
Control group:Hysteroscopic adhesion separation+uterine balloon placement+HRT
Sponsors
Women's Hospital School of Medicine Zhejiang University
Eligibility
Sex/Gender
Female
Age
20 Years to 40 Years
Inclusion criteria
Inclusion criteria: 1. Between 20 and 40 years old 2. Moderate to severe intrauterine adhesion (AFS score>5) 3. Subjects should have fertility requirements, possess good communication skills, and be able to cooperate for regular follow-up.
Exclusion criteria
Exclusion criteria: 1. Pregnancy 2. Abnormal vaginal bleeding or genital tract infection 3. Severe dysfunction of the liver, kidneys, heart, and lungs 4. Patients who are at a high risk for thrombosis 5. Combined with breast cancer 6. Combined with adenomyosis 7. Combined with endometriosis 8. Mild uterine adhesions
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| AFS score of intrauterine adhesions during the second hysteroscopy; | — |
Secondary
| Measure | Time frame |
|---|---|
| The endometrial morphological indexes and blood perfusion indexes measured during the first menstrual cycle after the second hysteroscopy;Rate of intrauterine pregnancy; | — |
Countries
China
Contacts
Public ContactYue Wang
Women's Hospital School of Medicine Zhejiang University
Outcome results
None listed