asymptomatic bacteriuria during pregnancy
Conditions
Interventions
Control group:Urine routine was monitored and signs of urinary tract irritation were observed according to the delivery procedures recommended by the national regulations and the Guidelines for Health
Observation group:Asymptomatic bacteriuria was managed, screened and treated
Sponsors
department of obstetrical, first affiliated hospital(army medical university)
Eligibility
Sex/Gender
Female
Age
16 Years to 35 Years
Inclusion criteria
Inclusion criteria: 1. Pregnant women who have established a pregnancy care manual in the obstetrics clinic of our hospital; 2. The 11-12 weeks of pregnancy were evaluated as low-risk pregnant women according to the "Chongqing Pregnancy Risk Assessment Table" (revised version). 1) No abnormalities in general condition (BMI=29 =18.5, no genital tract malformations, pelvic stenosis, deformed pelvis, thoracic deformities, etc.), 2) No pregnancy co-infected diseases (no gonorrhea, genital warts, syphilis infection, HIV infection, hepatitis B virus infection and other genital tract infections, etc.), 3) No history of abnormal pregnancy and childbirth (2 times of spontaneous abortion, 2 times of induced abortion<, 2 times of preterm birth, no history <of stillbirth, stillbirth, congenital anomalies, dystocia, macrosomia, postpartum hemorrhage), 4) no history of special surgery (no history of laparoscopic uterine surgery, cardiac surgery, transplantation, assisted reproductive technology pregnancy), 5) No medical comorbidities (no systemic lupus erythematosus, kidney disease, heart disease, abnormal liver function, fatty liver, recurrent asthma, cor pulmonale, diabetes, thyroid disease, epilepsy, intellectual disability, mental illness, etc.) 6) No contact with suspected teratogenic drugs, physical and chemical factors and viral infections in the first trimester. 3. Participate in the study voluntarily and sign the informed consent.
Exclusion criteria
Exclusion criteria: (1) scarred uterus; (2) Antibiotics or vaginal plugs have been used within two weeks; (3) Failure to understand the potential risks and benefits of the study, and failure to follow up and evaluate as required; (4) No capacity for civil conduct.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Genitourinary tract infection during pregnancy; | — |
Secondary
| Measure | Time frame |
|---|---|
| Preterm birth incidence;Incidence of abortion;Incidence of premature rupture of membranes; | — |
Countries
China
Contacts
Public ContactLiu Heying
first affiliated hospital(army medical university)
Outcome results
None listed