Maternal and Perinatal Outcome in Women With History of Premature Labor in Previous Pregnancy
Pregnancy, Vulvovaginitis, Uterine Cervicitis
About this trial
This is an interventional prevention trial for Pregnancy focused on measuring Pregnancy, vulvovaginitis, uterine cervicitis, pregnancy outcome
Eligibility Criteria
Inclusion Criteria:
- Will be included in the study women with a history of preterm labor in previous pregnancy, without other risk factors identified in the initial prenatal current to initiate prenatal care until 20 weeks of gestation in any unit of primary care and Botucatu they have agreed to participate.
Exclusion Criteria:
- Will be excluded from the study women who have complications during pregnancy such as urinary tract infections, severe periodontal disease, hypertension, diabetes or multiple gestation, among others.
Sites / Locations
Arms of the Study
Arm 1
Other
Active search of lower genital tract infections
Active search of lower genital tract infections Two groups (G1 and G2) will be part of study, each one composed of 140 pregnant women with a history of premature birth, G1 will have the active search and etiologic diagnosis of lower genital tract infections and G2 do not search of these infections, keeping for this group, the protocol of routine care of basic health units in the city of Botucatu. Workup care of pregnant women (G1) will include the completion of direct examination of vaginal contents stained by Gram's method, culture in the medium of Diamonds and polymerase chain reaction (PCR) of endocervical secretions, collected by health services in primary care the municipality in two moments: before 20th pregnancy week (M1) and in 36th pregnancy week (M2). The moment M3 will be after the birth, to evaluate the perinatal outcome.