recurrent spontaneous abortion
Conditions
Interventions
Two groups:Nil
Sponsors
Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine
Eligibility
Sex/Gender
Female
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: 1. Experimental group :clinical patients with RSA,excluding people with abnormal chromosome,anatomic abnormality,cryptorrheaor infection,et al.; 2. Control group:normal pregnant women in early time. Without the history of spontaneous abortion and stillbirth. And people without abnormal chromosome, anatomic abnormality,cryptorrhea or infection,et al. Without threatened abortion symptoms such as vaginal bleeding and abdominal pain during pregnancy, and ultrasound confirmed normal embryonic development.
Exclusion criteria
Exclusion criteria: 1. Having serve active infection; 2. couples with chromosome abnormalit; 3. having reproductive malformation; 4. taking medicine within one month; 5. people with?autoimmune disease.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| expression frequency of Bregs;surface molecular;cytokines; | — |
Countries
China
Contacts
Public ContactBao Shihua
Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine
Outcome results
None listed