Efficacy of Lactobacillus Rhamnosus LRa05 in Gestational Diabetes
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Conventional treatment and Probiotic.
- Who it may be relevant to
- Registry conditions: GDM. Basic parameters: 18 years — 50 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Assessing the Efficacy of Lactobacillus Rhamnosus LRa05 in Improving Blood Glucose and Gut Microbiota in Patients With Gestational Diabetes
Overview
This study aims to comprehensively evaluate the multifaceted impacts of Lactobacillus rhamnosus LRa05 on patients with gestational diabetes. Initially, the study will investigate the effects of LRa05 on improving patients' blood glucose levels and gut microbiota. Additionally, the study will assess the impact of this strain on patients' blood lipid levels, inflammatory markers, and body mass index (BMI). Furthermore, the study will also focus on its effects on thyroid function, vaginal microbiota, and bile acid metabolism in patients with gestational diabetes.
Interventions
- Dietary supplement Conventional treatment and Probiotic
Participants will continuously take Lactobacillus rhamnosus LRa05 from the time of enrollment until delivery.
Primary outcome measures
- Blood glucose change [Time frame: 16 weeks]
Eligibility criteria
Inclusion criteria
- Women diagnosed with gestational diabetes mellitus (GDM) at 24 weeks of gestation.
Diagnostic criteria for GDM: Abnormal oral glucose tolerance test (OGTT) with an 82.5g glucose load during the 24th week of pregnancy (defined as meeting one or more of the following plasma glucose thresholds: fasting ≥ 5.1 mmol/L, 1-hour ≥ 10 mmol/L, or 2-hour ≥ 8.5 mmol/L).
- Pregnant women aged 18 to 50 years.
- Singleton pregnancy with a fetus confirmed to be structurally and chromosomally normal via ultrasound or other prenatal diagnostic methods.
- No history of chronic diseases, including immune deficiency, hypertension, diabetes, kidney disease, or liver disease.
- No consumption of probiotic-containing foods (e.g., yogurt, fermented foods, soybean paste) within the two weeks prior to the study.
- Willing and able to provide written informed consent.
- Capable of complying with the study protocol and follow-up requirements.
Exclusion criteria
- Those who have taken items with similar functions to the test product in the short term, which may affect the judgment of the results.
- Those with other endocrine diseases or currently using medications that affect blood glucose control.
- Those with severe cardiovascular, kidney, or liver diseases.
- Those with immunodeficiency diseases or currently using immunosuppressive agents.
- Those with severe gastrointestinal diseases that may affect the absorption or metabolism of probiotics.
- Those currently using other medications that may affect blood glucose control or lipid levels.
- Those with a history of allergy to probiotics or any components of the study products.
- Those with unhealthy lifestyle habits, such as smoking, alcohol consumption, or drug abuse.
- Those who do not consume the test samples as required or do not follow up on time, resulting in uncertain efficacy.
- Study participants deemed unsuitable by other researchers.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Double blind
- Primary purpose
- Treatment
Study locations
China · 1 center
- Suzhou Municipal Hospital — Suzhou
Identifiers
NCT: NCT06901791 · WK20250321