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Published on: January 27, 2019
Lactobacillus-containing probiotics and clinical pregnancy in infertile women undergoing ART: a systematic review and
Daiki Hiratsuka1, Yasushi Hirota1
1Department of Obstetrics and Gynecology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Objective:
To assess whether Lactobacillus-containing probiotics improve clinical pregnancy in infertile women undergoing assisted reproductive technology (ART).
Methods:
We conducted a systematic review and meta-analysis (PROSPERO CRD420251149619). PubMed, Embase, and Web of Science were searched from Jan 1, 2005, to Oct 31, 2025 for full-text randomised controlled trials (RCTs) in infertile adult women undergoing ART that compared Lactobacillus-containing probiotics (vaginal or oral) with placebo or no supplementation before standard ART care. Two reviewers independently screened records, extracted published study-level data, and assessed risk of bias using RoB 2. We pooled risk ratios (RRs) using random-effects models (restricted maximum likelihood with Hartung-Knapp adjustment) and quantified heterogeneity with I2.
Results:
Seven RCTs (796 women; 399 probiotics, 397 control) were included. Probiotics were associated with higher clinical pregnancy than control (RR 1.49, 95% CI 1.07-2.07; I2 = 29%). In absolute terms, the pooled risk difference was 0·124 (95% CI 0·014-0·234), corresponding to approximately 12·4 additional clinical pregnancies per 100 women treated. The 95% prediction interval was 0·76-2·94. Effects were larger with treatment duration > 14 days (RR 1.99, 95% CI 1.44-2.75; I2 = 0%) than with ≤ 14 days (RR 1.16, 95% CI 0.67-2.00). Six trials were judged to be at low risk of bias and one was judged to have some concerns; adverse events were not reported in any included trial.
Conclusion:
Lactobacillus-containing probiotics may be associated with improved clinical pregnancy in women undergoing ART, particularly in trials using courses longer than two weeks. Larger, well-blinded multicentre RCTs evaluating live birth are needed to standardise clinically meaningful probiotic regimens and assess safety.
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