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Completed

NCT Number: NCT04721912

Group B Streptococcus Response After Probiotic Exposure

This is an open-label randomized control trial and feasibility study designed to determine the feasibility of a larger RCT in our setting that would examine prenatal probiotic use in Group B Strep (GBS) positive pregnant women at term. Investigators hope to address the question of whether prenatal oral probiotic use, taken by healthy low risk GBS positive women from approximately 37 weeks gestation until the time of birth, will reduce the number of women who test positive for GBS at the time of admission to Labor and Delivery (L&D).

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

Primary location

University of New Mexico Hospital

Albuquerque, New Mexico, 87112, United States

About this study

This is an open-label randomized control trial and feasibility study designed to determine the feasibility of a larger RCT in our setting that would examine prenatal probiotic use in Group B Strep (GBS) positive pregnant women at term. We hope to address the question of whether prenatal oral probiotic use, taken by healthy low risk GBS positive women from approximately 37 weeks gestation until the time of birth, will reduce the number of women who test positive for GBS at the time of admission to Labor and Delivery (L&D). In this study we aim to determine whether such a study is acceptable in our population, whether any adverse events are identified, and what barriers or confounding variables might exist to probiotic use at term. We will also look at whether probiotic use had any reported effect on maternal gastrointestinal (GI) symptoms.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy adult (≥ 18 years of age) pregnant women who are 36 - 37 6/7 weeks gestation at enrollment [calculated from the first day of Last Normal Menstrual Period (LNMP) and/or ultrasound (US)]

Group B Streptococcus Positive at 36 weeks gestation with:

  • No obstetric complication requiring delivery prior to 39 weeks (hypertensive disorder diagnosed prior to enrollment, gestational diabetes, multiple gestation)
  • No fetal complication (e.g., birth defect, intrauterine growth restriction)
  • No medical complication (e.g., chronic hypertension, preexisting diabetes mellitus)
  • Who do not currently ingest an over the counter probiotic supplement (not including yogurt)
  • Who can both speak and read English or Spanish
  • Pregnant women who regularly attend UNM prenatal clinics for their prenatal care ("regularly attend" will be defined as starting prenatal care prior to 20 weeks gestation and missing no more than one prenatal appointment during this pregnancy)
  • No hypersensitivity reaction to β-lactam antibiotics

Exclusion criteria

  • Those less than 18 years of age
  • Non-pregnant women
  • Later in pregnancy than 38 weeks gestation at enrollment [per LNMP and/or US]
  • Those with an obstetric, fetal or medical complication of pregnancy
  • Group B Streptococcus negative at 36 weeks gestation. Those ineligible for testing at 36 weeks gestation (history of GBS bacteriuria during the current pregnancy or have previously given birth to a GBS affected child.) We will not exclude those with bacteriuria other than GBS, and we will not exclude women who have taken an antibiotic during pregnancy, but we will track this as it is addressed in the Questionnaire for Women.
  • Women who are currently ingesting an over the counter probiotic supplement (except for yogurt)
  • Women who do not have electricity in the home.
  • Women who are planning an elective repeat cesarean birth
  • Women who do not speak and read English or Spanish
  • Women with a history of missing one or more scheduled prenatal visit during this pregnancy
  • Hypersensitivity reaction to β-lactam antibiotics

Treatment and study plan

Probiotic dietary supplement

Drug

GBS positive patients, at ≥ 36 weeks gestation, will begin taking oral Florajen Digestion probiotic capsules once daily from time of enrollment/randomization at ≥ 36 weeks gestation until the time of birth.

Other names: Florajen Digestion™

Primary outcomes

  1. GBS Culture Result (Positive Versus Negative)

    Time frame: T2 (admission to Labor and Delivery; 36 - 42 weeks gestational age)

    Qualitative GBS colonization (positive versus negative)

Secondary outcomes

  1. Probiotic Pill Count to Measure Intervention Adherence

    Time frame: T3 (Postpartum day 0-14, up to 8 weeks from Baseline)

    Intervention adherence by pill count for probiotic participants

  2. Antepartum Gastrointestinal Symptom Assessment (AP-GI-SA) Score

    Time frame: Baseline T1 (36-37.6 weeks gestational age) and T3 (postpartum day 0-14; up to 8 weeks from baseline)

    Maternal gastrointestinal (GI) symptoms based on AP-GI-SA score: lowest score 10, highest score 50 (high score means more symptoms = worse outcome)

  3. Number of Participants Who Report Adverse Events

    Time frame: T1 (baseline; 36.0-37.6 weeks gestational age) through T5 (6 weeks postpartum visit; up to 12 weeks and 6 days from baseline)

    Maternal adverse events by organ system and severity.

  4. Number of Participants Who Report Adverse Events in Their Infant

    Time frame: T2 (admission to Labor and Delivery; 36 - 42 weeks gestational age) through T5 (6 weeks postpartum visit; up to 12 weeks and 6 days from baseline)

    Infant adverse events by organ system and severity

Sponsors and collaborators

Lead sponsor

University of New Mexico

Other

Collaborators

  • Marquette University

Registry information

Official study title

Open-label Randomized Control Trial and Feasibility Study of Florjajen Digestion Probiotics to Reduce GBS Colonization in Pregnant Women by the Time of Birth.

Acronym: GRAPE

Important dates

Study start
2020
Primary completion
2023
Study completion
2023
First posted
Jan 25, 2021
Registry last updated
Jan 14, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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