The purpose of this study is to examine the effect of lactobacillus preparation on Bacterial vaginosis (BV) in low-risk pregnant women and to evaluate the value of double courses for the patients with durative positive result. It is assumed that the living preparation of lactobacillus was beneficial for treatment of BV during pregnancy. The two-courses treatment can increase the response rate and improve pregnancy outcomes in the durative BV positive patients comparing with one-course one.
Research method: This was a single-blind randomized controlled trial. Diagnostic standard: The study population is the women who have positive outcome of screened test for BV by sialidase method. Allocation and follow up: Patients who were screened for BV by sialidase method and randomly allocated into control group、one-course group and two-course group. The patients in control group who were BV positive would receive lotion washout and be repeatedly evaluated BV status per two weeks and be followed up to the 4th~7th days of postpartum. The patients in one-course group and in two-course group who were BV positive would receive the first course treatment of vaginal lactobacillus capsule and be repeatedly evaluated BV status after treatment. The patients in two-course group will receive the second course treatment of Lactobacilli preparation if their BV test result were still positive after one-course treatment, but those in one-course group would NOT receive any treatment even though they would have the durative BV positive result after one-course of Lactobacilli. The patients in the two interventional groups would be repeatedly evaluated BV status at 28th gestational weeks and be followed up to the 4th-7th days of postpartum. All the inspection results of vaginal secretions and pregnancy outcome were recorded. Outcome measures: * The prevalence of BV,the response rates of lactobacillus preparation,the recurrence rate. * The adverse pregnancy outcomes of mother. * The adverse pregnancy outcomes of perinatal fetus.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
5,000
The patients in one-course group who were BV positive would receive the first course treatment of vaginal lactobacillus capsule and be repeatedly evaluated BV status after treatment. If their BV test result were still positive after one-course treatment, they would NOT receive any treatment but would be followed up to the 4th-7th days of postpartum.
The patients in two-course group who were BV positive would receive the first course treatment of vaginal lactobacillus capsule and be repeatedly evaluated BV status after treatment. If their BV test result were still positive after one-course treatment, they will receive the second course treatment of Lactobacilli preparation.
Maternal and child care hospital in Panyu District
Guangzhou, Guangdong, China
RECRUITINGNumber of Participants who transformed to negative status of bacterial vaginosis
The patients who were BV positive would receive treatment and be repeatedly evaluated BV status on the time of post-treatment 1 week, 28th gestational weeks, and before birth, respectively.The number of Participants who transformed to negative status of bacterial vaginosis will be recorded. The rates of bacterial vaginosis transformed to negative status will be calculated.
Time frame: 6 months
pregnancy outcome of mother
1. the delivery weeks 2. the delivery mode 3. the presence of premature rupture of fetal membra 4. the presence of premature labor 5. the volume of postpartum haemorrhage 6. the presence of pregnancy complications 7. the highest temperature during the first three days of postpartum
Time frame: 6 months (from 16~18 gestational weeks to the 4th-7th days of postpartum)
pregnancy outcome of perinatal fetus
1. the neonatal birth weight 2. the presence of fetal distress 3. the neonatal 1 min Apgar score 4. the numerically highest value of neonatal transcutaneous bilirubinometry
Time frame: 6 months (from 16~18 gestational weeks to the 4th-7th days of postpartum)
Safety and tolerability
1. liver function test 2. renal function test
Time frame: 6 months (from 16~18 gestational weeks to the 4th-7th days of postpartum)
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