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Effect of Different Courses of Lactobacilli Treatment on Bacterial Vaginosis and Pregnancy Outcomes (BV)

Primary Purpose

Bacterial Vaginosis

Status
Unknown status
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
Vaginal capsules of lactobacilli
Vaginal capsules of lactobacilli
Sponsored by
The First Affiliated Hospital, Guangzhou University of Traditional Chinese Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bacterial Vaginosis focused on measuring Bacterial vaginosis, Probiotics, Lactobacilli, Pregnancy outcome, Randomized controlled trial

Eligibility Criteria

20 Years - 50 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • pregnant women at 16-18 gestational weeks with no history of premature labor or premature rupture of fetal membranes.

Exclusion Criteria:

  • who have menstrual disorder or forget the last menstrual period, and have no type-B ultrasonic result, so the gestational week is not clear.
  • Who have monilial vaginitis, trichomonas vaginitis, or sexual transmitted diseases.
  • who have severe medicochirurgic diseases.
  • multiple pregnancy.
  • anomalies of genital tract
  • fetal anomaly

Sites / Locations

  • Maternal and child care hospital in Panyu DistrictRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Placebo Comparator

Experimental

Experimental

Arm Label

lotion

lactobacilli capsule

lactobacilli capsules

Arm Description

lotion:the patients in control group receive washing medicine and are followed up to the 4rd~7th days of postpartum.

Outcomes

Primary Outcome Measures

Number 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.

Secondary Outcome Measures

pregnancy outcome of mother
the delivery weeks the delivery mode the presence of premature rupture of fetal membra the presence of premature labor the volume of postpartum haemorrhage the presence of pregnancy complications the highest temperature during the first three days of postpartum
pregnancy outcome of perinatal fetus
the neonatal birth weight the presence of fetal distress the neonatal 1 min Apgar score the numerically highest value of neonatal transcutaneous bilirubinometry
Safety and tolerability
liver function test renal function test

Full Information

First Posted
August 8, 2011
Last Updated
August 22, 2011
Sponsor
The First Affiliated Hospital, Guangzhou University of Traditional Chinese Medicine
Collaborators
Ministry of Health, China
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1. Study Identification

Unique Protocol Identification Number
NCT01421615
Brief Title
Effect of Different Courses of Lactobacilli Treatment on Bacterial Vaginosis and Pregnancy Outcomes
Acronym
BV
Official Title
Effect of Different Courses of Lactobacilli Treatment on Bacterial Vaginosis and Related Pregnancy Outcomes
Study Type
Interventional

2. Study Status

Record Verification Date
August 2011
Overall Recruitment Status
Unknown status
Study Start Date
January 2011 (undefined)
Primary Completion Date
December 2011 (Anticipated)
Study Completion Date
May 2012 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The First Affiliated Hospital, Guangzhou University of Traditional Chinese Medicine
Collaborators
Ministry of Health, China

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bacterial Vaginosis
Keywords
Bacterial vaginosis, Probiotics, Lactobacilli, Pregnancy outcome, Randomized controlled trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
Participant
Allocation
Randomized
Enrollment
5000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
lotion
Arm Type
Placebo Comparator
Arm Description
lotion:the patients in control group receive washing medicine and are followed up to the 4rd~7th days of postpartum.
Arm Title
lactobacilli capsule
Arm Type
Experimental
Arm Title
lactobacilli capsules
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Vaginal capsules of lactobacilli
Other Intervention Name(s)
Brand names: Dingjunsheng, Commodity code name: A246912309879, Approved by the state: S20030005
Intervention Description
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.
Intervention Type
Drug
Intervention Name(s)
Vaginal capsules of lactobacilli
Other Intervention Name(s)
Brand names: Dingjunsheng, Commodity code name: A246912309879, Approved by the state: S20030005
Intervention Description
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.
Primary Outcome Measure Information:
Title
Number of Participants who transformed to negative status of bacterial vaginosis
Description
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
Secondary Outcome Measure Information:
Title
pregnancy outcome of mother
Description
the delivery weeks the delivery mode the presence of premature rupture of fetal membra the presence of premature labor the volume of postpartum haemorrhage the presence of pregnancy complications 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)
Title
pregnancy outcome of perinatal fetus
Description
the neonatal birth weight the presence of fetal distress the neonatal 1 min Apgar score the numerically highest value of neonatal transcutaneous bilirubinometry
Time Frame
6 months (from 16~18 gestational weeks to the 4th-7th days of postpartum)
Title
Safety and tolerability
Description
liver function test renal function test
Time Frame
6 months (from 16~18 gestational weeks to the 4th-7th days of postpartum)

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: pregnant women at 16-18 gestational weeks with no history of premature labor or premature rupture of fetal membranes. Exclusion Criteria: who have menstrual disorder or forget the last menstrual period, and have no type-B ultrasonic result, so the gestational week is not clear. Who have monilial vaginitis, trichomonas vaginitis, or sexual transmitted diseases. who have severe medicochirurgic diseases. multiple pregnancy. anomalies of genital tract fetal anomaly
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yanfang LEE
Phone
13928777126
Email
13928777126@139.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yanfang Lee, Master
Organizational Affiliation
The First Affiliated Hospital of Guangzhou University of TCM
Official's Role
Principal Investigator
Facility Information:
Facility Name
Maternal and child care hospital in Panyu District
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
511400
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yanfang LEE
Phone
13928777126
Email
13928777126@139.com
First Name & Middle Initial & Last Name & Degree
Yanfang LEE

12. IPD Sharing Statement

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Effect of Different Courses of Lactobacilli Treatment on Bacterial Vaginosis and Pregnancy Outcomes

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