University of New Mexico Hospital
Albuquerque, New Mexico, 87112, United States
NCT Number: NCT04721912
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).
Looking for future studies?
Notify Me18 year and older
Female
Interventional
Phase 3
Albuquerque, New Mexico, 87112, United States
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Group B Streptococcus Positive at 36 weeks gestation with:
Exclusion criteria
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™
Time frame: T2 (admission to Labor and Delivery; 36 - 42 weeks gestational age)
Qualitative GBS colonization (positive versus negative)
Time frame: T3 (Postpartum day 0-14, up to 8 weeks from Baseline)
Intervention adherence by pill count for probiotic participants
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)
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.
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
University of New Mexico
Other
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
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.
Published trials that share one or more normalized conditions with this study.
NCT03807245
Bacterial Infections, Bacterial Infections and Mycoses
Merthyr Tydfil, Wales, United Kingdom
View Trial DetailsNCT07562061
Bacterial Infections, Bacterial Infections and Mycoses
Kampala, Uganda
View Trial DetailsNCT04549220
Bacterial Infections, Bacterial Infections and Mycoses
Kampala, Uganda
View Trial DetailsNCT04596878
Bacterial Infections, Bacterial Infections and Mycoses
Johannesburg, South Africa
View Trial Details