Effects of Oral Probiotic Supplementation on Group B Strep (GBS) Rectovaginal Colonization in Pregnancy

Oral Probiotic Supplementation and Group B Streptococcus Rectovaginal Colonization in Pregnant Women: a Randomized Double-blind Placebo-controlled Trial.

The investigators wish to determine if oral probiotic supplementation during the second half of pregnancy decreases maternal GBS recto-vaginal colonization at 35-37 weeks' gestational age, thereby decreasing need for maternal antibiotic administration at time of labor. The importance of this study is that it may offer a safer alternative to antibiotic treatment of group B Streptococcus (GBS) colonized pregnant women.

Study Overview

• Status: Completed
• Conditions: Pregnancy; Infection
• Intervention / Treatment: Dietary supplement: Probiotic dietary supplement; Drug: Placebo

Detailed Description

1. Screening: All pregnant women prior to 28 weeks gestational age. Patients who choose to enroll and who will not deliver at Lucile Packard Childrens Hospital at Stanford will sign release of medical information forms for study personnel to access pregnancy outcomes. Patients receiving obstetric care at any of the satellite research sites in Santa Cruz will also be offered enrollment in the study.
2. Women will continue regular and routine obstetric care and clinic visits.
3. Placebo vs probiotic daily regimen: We plan to begin administration of product and placebo at 20 weeks gestation, and no later than 28 weeks gestation until delivery. Once a women is enrolled in the study, she will be randomized to either the placebo or the probiotic group.
4. At the time of randomization, the patient will receive her month supply of 30 capsules; The allocation arm will be double-blinded.
5. The investigators will schedule the women for routine monthly obstetric visits (more often if clinically required) during which time they will also meet with one of the investigators. The investigator at each monthly visit will provide an additional monthly allotment of 30 capsules. The capsule bottle from the previous cycle will be collected and dated if there are capsules remaining in the bottle. Remaining capsules will be counted and refrigerated for future use.
6. The investigators will collect history data including safety data per the questionnaire and will document compliance with the study.
7. GBS recto-vaginal screening: The investigators will enroll the women in the study and we will perform the standard GBS colonization screening (using standard GBS recto-vaginal cultures) at 36 weeks.
8. Additionally, subjects may opt to have serial vaginal swabs collected to assess potential beneficial effects of probiotics on the vaginal microbiota and bacterial vaginosis (BV) status. Vaginal swabs will be collected (either by study personnel or self-collected by the study participant). Swabs will be inserted 1-2 inches into the vaginal introitus and spun for 20 seconds and then withdrawn. Swabs will be collected at the following time points: prior to probiotic/placebo initiation, every 1-4 weeks from time of enrollment to time of delivery, and postpartum serially up to 12 months. These swabs will be stored at -20 degrees Celsius or colder for additional microbiologic analyses.
9. Additionally, placental tissue may be collected at time of delivery for possible future microbiome and/or other analyses.
10. Women who suffer a premature rupture of the membranes, deliver before 36 weeks gestation, or go into labor before the GBS culture result is available, will receive the standard GBS antibiotic prophylaxis.
11. Labor: The patient will receive standard delivery and newborn care. Patients with a positive GBS culture will be treated with standard antibiotics in labor.
12. Postpartum and neonatal care: The patient will receive routine postpartum care per the obstetric team. Data regarding her postpartum course and neonatal outcomes will be collected.

• Study Type: Interventional
• Enrollment (Actual): 251
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • California
    • Aptos, California, United States, 95003
      • Aptos Women's Health Center
    • Santa Cruz, California, United States, 95065
      • Dominican Hospital
    • Stanford, California, United States, 94305
      • Stanford University School of Medicine/Lucile Packard Children's Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 55 years (ADULT)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: Female

Description

Inclusion Criteria:

1. Pregnant women between 20-28 weeks gestation.
2. 18 years of age or older.
3. Singleton gestation.

Exclusion Criteria:

1. Preexisting morbidity: Immunocompromised status (HIV +; malignancy; history of organ transplant; chronic steroid therapy; autoimmune disease requiring treatment during pregnancy, and other immunocompromised states); Type 1 diabetes and type 2 diabetes;congenital cardiac disease and cardiac valvular disease requiring antibiotic prophylaxis during procedure/labor; pulmonary disease (except mild asthma); renal disease; chronic hepatic disease (Hepatitis B, C); inflammatory bowel disease (Crohn's disease or ulcerative colitis); stomach or duodenal ulcer; bowel resection, gastric bypass, and chronic indwelling venous, bladder, or gastric catheter.
2. Multi-fetal gestation.
3. Use of probiotics preparations in the 3 months prior to beginning of the study treatment or use of any additional probiotics preparations (other than study treatment) at any time during the study period (including over the counter food supplements such as Activia, BioK, other oral or vaginal probiotics products (BUT not including other common forms of yogurt).
4. Chronic (daily) use of broad spectrum antibiotics.
5. History of infant with GBS sepsis.
6. Intrauterine Growth Restriction (IUGR), Fetal Anomalies-major diagnosed at time of second trimester anatomy ultrasound
7. Anticipated delivery <35 wks for maternal/fetal indication
8. Placenta previa or accreta (with anticipated delivery prior to 35 weeks)

Study Plan

How is the study designed?

Design Details

• Primary Purpose: PREVENTION
• Allocation: RANDOMIZED
• Interventional Model: PARALLEL
• Masking: QUADRUPLE

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
ACTIVE_COMPARATOR: Probiotic dietary supplement; Probiotic dietary supplement one capsule once per day until delivery.	Dietary supplement: Probiotic dietary supplement; Dietary Supplement: Lactobacillus rhamnosus GR-1, Lactobacillus reuteri RC -14; Other Names: Other Names:; Jarrow's fem-dophilus
PLACEBO_COMPARATOR: Placebo; Placebo capsule, one daily until delivery.	Drug: Placebo; One placebo capsule daily.; Other Names: Sugar pill

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Count of Participants With Positive Group B Streptococcus Rectovaginal Colonization Status at 35- 37 Weeks' Gestational Age	Gestational age is given in a format of full weeks.	35 to 37 weeks gestational age

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Count of Participants With Urinary Tract Infection		From enrollment up to delivery hospitalization (up to 42 weeks gestation)
Count of Participants With Intrapartum Chorioamnionitis	Intrapartum chorioamnionitis is maternal temperature above 38.0 degrees Celsius and one or more of the following findings: fetal tachycardia; maternal tachycardia; uterine tenderness; purulent or malodorous amniotic fluid, or elevated maternal white blood cell count.	From time of labor onset until delivery (up to 42 weeks of gestation)
Count of Participants With Endometritis	Endometritis is a uterine (myometrial) infection.	From time of delivery up to 6 weeks postpartum
Count of Participants With Cellulitis	Cellulitis is a bacterial skin infection.	From time of delivery up to 6 weeks postpartum
Count of Participants With Bacteremia	Bacteremia is defined as presence of bacteria in the blood.	From time of labor onset up to 6 weeks postpartum
Count of Participants With Sepsis	Sepsis is defined as life-threatening organ dysfunction caused by a dysregulated response of the body to an infection.	From labor onset up to 6 weeks postpartum
Count of Participants With Other Infectious Morbidity	Other infectious morbidity included maternal mastitis or pneumonia.	From time of labor onset up to 6 weeks postpartum
Gestational Age at Delivery	Gestational age at delivery is presented as weeks.	At time of delivery (up to 42 weeks of gestation)
Apgar Score at 1 and 5 Minutes Following Delivery	Apgar score is a measure to quickly assess the neonatal health status from time of delivery. Score ranges from 0-10. Lower scores correspond to worse health state; neonates with scores below 5 are considered to have poor prognosis.	At time of delivery (up to 42 weeks of gestation)
Neonatal Bilirubin Level		Up to 14 days following delivery
Neonatal C-reactive Protein Level	Maximum neonatal C-reactive protein level	Up to 14 days following delivery
Count of Neonates Requiring a "Rule-out Sepsis Evaluation"	Outcome was based on performance of neonatal blood culture.	Up to 14 days following delivery
Count of Neonates With Sepsis		Up to 14 days following delivery
Count of Neonates With Pneumonia		Up to 14 days following delivery
Count of Neonates With Meningitis		Up to 14 days following delivery
Count of Neonates With Intensive-care Unit Admission		Up to 14 days following delivery
Length of Neonatal Hospital Stay		Up to 14 days following delivery

Collaborators and Investigators

• Sponsor: Stanford University
• Investigators: Principal Investigator: Natali Aziz, MD, Stanford University School of Medicine/Lucile Packard Children's Hospital

Study record dates

Study Major Dates

• Study Start: November 1, 2011
• Primary Completion (ACTUAL): July 26, 2017
• Study Completion (ACTUAL): July 26, 2017

Study Registration Dates

• First Submitted: November 22, 2011
• First Submitted That Met QC Criteria: November 23, 2011
• First Posted (ESTIMATE): November 24, 2011

Study Record Updates

• Last Update Posted (ACTUAL): August 20, 2018
• Last Update Submitted That Met QC Criteria: August 14, 2018
• Last Verified: August 1, 2018

More Information

Terms related to this study

• Other Study ID Numbers: 18840

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO