Intrauterine adhesions
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Aged 25–45 years. 2. Diagnosed with inevitable abortion at 6–12 weeks of gestation, with chromosomal testing required for the products of conception after uterine evacuation. 3. Voluntary participation in the study with signed informed consent. If the participant is unable to read the informed consent form (e.g., illiterate participants), an impartial witness must observe the consent process and co-sign the document.
Exclusion criteria
Exclusion criteria: 1. Patients who have not undergone ultrasound examination within 2 weeks after uterine evacuation. 2. Patients with autoimmune or infectious diseases, including hepatitis B, syphilis, systemic lupus erythematosus (SLE), etc. 3. Vulnerable populations (other than illiterate individuals and pregnant women), such as those with mental illness, cognitive impairment, critical illness, or minors.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intrauterine adhesions;Endometrial thickness; | — |
Countries
China
Contacts
Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University