NCT04335656Active, not recruitingPhase 2
Reducing Innate Inflammation in New Onset Type 1 Diabetes
Reducing Innate Inflammation in New Onset Type 1 Diabetes With Lactiplantibacillus Plantarum
Source: ClinicalTrials.gov · Last updated 20 Oct 2026
Brief summary (registry, in English)
This study aims to determine whether Lactiplantibacillus plantarum 299v (Lp299v) supplementation will reduce systemic inflammation and prolong residual beta cell function in individuals newly diagnosed with Type 1 diabetes. The investigators hypothesize that probiotic-induced alterations in the intestinal microbiota may favorably alter the post-onset disease state.
- Status (registry)
- Active, not recruiting
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 51 (actual)
- First submitted
- 27 Mar 2020
- Start date
- 1 Apr 2021
- Primary completion date
- 31 Dec 2026
- Lead sponsor
- Medical College of Wisconsin
- Diseases
- Type 1 diabetes
- NCT number
- NCT04335656
What you commit to
- Study type: Interventional · Phase 2
- Participants enrolled: 51
- From 1 Apr 2021 to the primary completion date, 31 Dec 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Concurrent or recent (within the past 30 days of screening) use of non-insulin therapies aimed to control hyperglycemia
Other illness
- Chronic inflammatory or autoimmune disease with exception of stable thyroid disease
- Uncontrolled celiac disease (i.e., consuming gluten) or actively being evaluated for possible celiac disease (i.e., clinically obtained tissue transglutaminase IgA titers above reference range, being referred to gastroenterology for possible endoscopy, etc.)
- Dairy allergy
- Any condition that, in the investigator's opinion, may compromise study participation or may confound the interpretation of the study results.
Lab values
- Use of medications known to influence glucose tolerance
Other
- Probiotic supplement use within the past month
- Antibiotic use within the past month
- Females who are pregnant or lactating
- Use of glucocorticoids or other immunosuppressive agents within 30 days of screening MMTT
Who the study is looking for
- ≤ 100 days from T1D diagnosis based on ADA criteria
- \> 21 days from T1D diagnosis or metabolically stable per study physician assessment
- Males and females 3-45 years of age, inclusive, at time of screening visit
- Peak MMTT stimulated C-peptide ≥ 0.2 nmol/L
- Positive for at least 1 diabetes autoantibody (excluding mIAA in those who have received ≥ 2 weeks of exogenous insulin therapy) either through clinically obtained labs at time of diagnosis or as obtained at the screening visit
- Females of child-bearing potential (defined as any female who has reached menarche (first menses), excluding those who have had a hysterectomy or are post-menopausal and must be willing to use effective birth control (which may include abstinence)) from screening visit until final study visit
- Willing and able to give informed consent or have parent or legal guardian provide informed consent if the subject is \< 18 years of age
Age in the registry: 3 years to 45 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Medical College of Wisconsin Coordinator of this site? Confirm its status | Milwaukee | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.