None
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Singleton intrauterine pregnancy; 2. Age>=18 years old; 3. Voluntary and able to participate in this study independently. Among them, the observation group had additional inclusion criteria: pre-pregnancy body mass index (BMI) >=25kg/m^2; and the control group had additional inclusion criteria: pre-pregnancy body mass index (BMI) <25kg/m^2.
Exclusion criteria
Exclusion criteria: 1. Patients with hypertension, diabetes, cardiovascular disease, thyroid disease, blood disease and polycystic ovary syndrome before pregnancy, pregnancy infection, multiple pregnancy; 2. Severe heart, brain, liver and kidney insufficiency during pregnancy; 3. The time of loss to follow-up is greater than 3 months; 4. Those who cannot give their consent voluntarily due to other reasons.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fasting blood glucose;hemoglobin;uric acid;triglyceride;cholesterol;High density lipoprotein;Low density lipoprotein;albumin; | — |
Countries
China
Contacts
Hangzhou Xiaoshan District Second People's Hospital