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Probiotics Capsule as Supplemental Therapy for Group B Streptococci Infection and Vaginitis During Pregnancy

Primary Purpose

Pregnancy

Status
Unknown status
Phase
Phase 4
Locations
Taiwan
Study Type
Interventional
Intervention
lactic acid bacteria
cranberry
placebo
Sponsored by
Meng-Hsing Wu
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pregnancy focused on measuring group B streptococcus, pregnancy, probiotics

Eligibility Criteria

20 Years - 50 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • pregnancy women at 35 weeks of gestation

Exclusion Criteria:

  • previous other probiotics capsules use
  • previous antibiotics use
  • previous habitual vaginal douche
  • previous medical disease, such as: HIV infection, cancer, history of organ transplantation, long-term steroid use, autoimmune disease, et al

Sites / Locations

  • Department of Obstetrics and Gynecology, College of Medicine, National Cheng Kung UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Placebo Comparator

Arm Label

latic acid bacteria and cranberry

cranberry

placebo

Arm Description

oral latic acid bacteria and cranberry capsule (dose of 2 * 10^9 cfu per capsule), one pill daily

oral cranberry capsule without lactic acid bacteria, one pill daily

placebo without lactic acid bacteria and cranberry, one pill daily

Outcomes

Primary Outcome Measures

all cases vaginal group B streptococcus colonies

Secondary Outcome Measures

Full Information

First Posted
January 28, 2013
Last Updated
April 26, 2015
Sponsor
Meng-Hsing Wu
Collaborators
National Cheng-Kung University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01779193
Brief Title
Probiotics Capsule as Supplemental Therapy for Group B Streptococci Infection and Vaginitis During Pregnancy
Official Title
A Double-blind,Randomized,Parallel,Placebo-controlled Study of Probiotics Capsule as Supplemental Therapy for Group B Streptococci Infection and Vaginitis During Pregnancy
Study Type
Interventional

2. Study Status

Record Verification Date
April 2015
Overall Recruitment Status
Unknown status
Study Start Date
June 2012 (undefined)
Primary Completion Date
July 2015 (Anticipated)
Study Completion Date
July 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Meng-Hsing Wu
Collaborators
National Cheng-Kung University Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
B streptococcal infection and the major cause of death before and after the baby is born. B streptococcus infection the way of the newborn, usually infection from the mother in childbirth, if the pregnant women during pregnancy early diagnosis B streptococcus infection, it can be effective in preventing the risk of neonatal infection. Department of Health in China has been since April 15, 2012, the Scholarship holder at all pregnant women in the 35-37 weeks of pregnancy comprehensive B streptococcus screening. Infection B Streptococcus pregnant women in the labor process, the use of prophylactic antibiotics can be effective in reducing neonatal B streptococcus infection, but the possibility of the fetus being infected for the condition of premature birth or early rupture of membranes are still unable to fully hedge. In this study, the 35 to 37 weeks gestation examination confirmed infected B Streptococcus pregnant women, oral lactobacillus capsules B streptococcus infection treatment efficacy and safety assessment of clinical research. To assess whether oral administration of lactic acid bacteria will affect vaginitis incidence.
Detailed Description
Deeply influenced of bacterial vaginosis infection during pregnancy for pregnant women and fetus during childbirth, in which Group B Streptococcus agalactiae(GBS) is generally about 30% of pregnant women will be infected, about 1% vertical and infect the fetus, babies are not infected about 50% of the mortality rate in the treatment status, is considered an important reason for infection and death before and after the baby is born. Vertically in the natural childbirth process and infect the fetus, the delay in treatment on the fetus often lead to serious complications, including sepsis, pneumonia and meningitis, a serious will to cause death and permanent neurological sequelae, if given to confirm the diagnosis antibiotic treatment of pregnant women, the probability of infection of the newborn B streptococcus can be reduced by 75%. U.S. Centers for Disease Control recommends that pregnant women 35 to 37 weeks gestation or less than 37 weeks preterm contractions or rupture of membranes. B streptococcus check preterm doubts should pregnant women in the labor process and the use of preventive antibiotics can be effective in reducing neonatal B streptococcus infection, but the condition of premature birth or early rupture of membranes can not fully prevent the possibility of the fetus being infected is still in pre-production will not make any disposal, can cause infection of B The streptococci pregnant women worry, and under great pressure. This study for 35 to 37 weeks gestation to check to confirm infection of B Streptococcus pregnant women, pregnant women infected with the clinical studies of treatment efficacy and safety assessment of B streptococcus before delivery to the oral administration of lactic acid bacteria. The trial is expected during the execution in June 2012 to July 2015, subjects the number is expected to included at least 120 pregnant women choose not to subjects according to the conventional injection of prophylactic antibiotics in the labor process, choose to take oral lactobacillus oral lactobacillus of pregnant women in accordance with the 1:1 double-blind randomized to three groups, one of the following: test group A: oral lactobacillus capsules (dose of 2 x 109 cfu / capsule), experimental group B: oral without functional lactobacillus capsules and the control group: oral administration does not contain the active ingredient (lactic acid bacteria and cranberry) capsules before oral administration of lactic acid bacteria and the delivery process, collecting samples of vaginal anal secretions, whether positive addition to the screening B streptococcus, and the other selective medium coated plate culture for vaginal odor, itching number of the pathogen and B Streptococcus quantitative analysis and assessment questionnaire.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pregnancy
Keywords
group B streptococcus, pregnancy, probiotics

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
latic acid bacteria and cranberry
Arm Type
Experimental
Arm Description
oral latic acid bacteria and cranberry capsule (dose of 2 * 10^9 cfu per capsule), one pill daily
Arm Title
cranberry
Arm Type
Active Comparator
Arm Description
oral cranberry capsule without lactic acid bacteria, one pill daily
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
placebo without lactic acid bacteria and cranberry, one pill daily
Intervention Type
Dietary Supplement
Intervention Name(s)
lactic acid bacteria
Intervention Description
oral lactobacillus capsule (dose of 2 * 10^9 cfu per capsule), one pill daily
Intervention Type
Dietary Supplement
Intervention Name(s)
cranberry
Intervention Description
oral cranberry capsule, one pill daily
Intervention Type
Dietary Supplement
Intervention Name(s)
placebo
Intervention Description
placebo capsule without lactic acid bacteria and cranberry, one pill daily
Primary Outcome Measure Information:
Title
all cases vaginal group B streptococcus colonies
Time Frame
four years

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: pregnancy women at 35 weeks of gestation Exclusion Criteria: previous other probiotics capsules use previous antibiotics use previous habitual vaginal douche previous medical disease, such as: HIV infection, cancer, history of organ transplantation, long-term steroid use, autoimmune disease, et al
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Meng-Hsing Wu, M.D., Ph.D.
Phone
+88662353535
Ext
5222
Email
mhwu68@mail.ncku.edu.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Meng-Hsing Wu, M.D., Ph.D.
Organizational Affiliation
National Cheng Kung University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Obstetrics and Gynecology, College of Medicine, National Cheng Kung University
City
Tainan
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Meng-Hsing Wu, M.D., Ph.D.
Phone
+88662353535
Ext
5222
Email
mhwu68@mail.ncku.edu.tw
First Name & Middle Initial & Last Name & Degree
Meng-Hsing Wu, M.D., Ph.D.

12. IPD Sharing Statement

Learn more about this trial

Probiotics Capsule as Supplemental Therapy for Group B Streptococci Infection and Vaginitis During Pregnancy

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