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Improvement and therapeutic effect of Lactobacillus paracasei on autoimmune status in patients with type 1 diabetes mellitus

Improvement and therapeutic effect of Lactobacillus paracasei on autoimmune status in patients with type 1 diabetes mellitus

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075613
Enrollment
Unknown
Registered
2023-09-11
Start date
2023-09-11
Completion date
Unknown
Last updated
2023-09-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 1 diabetes

Interventions

Treatment group:Lactobacillus paracasei + diabetic basic treatment program

Sponsors

Sir Run Run Hospital, Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
13 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. According to the World Health Organization (WHO) disease diagnostic criteria classification T1D; 2. Age =13 years old, gender unlimited; 3. Course of T1D disease =5 years; 4. Retain certain islet function, defined as fasting C-peptide >100 pmol/L[0.30 ng/mL] or random C-peptide >200 pmol/L[0.60 ng/mL]); 5. Able and willing to perform the following procedures as determined by the investigator: self-glucose monitoring (SMBG); Fill in the patient log as required; Diabetes education is available; Research treatment and research visits that comply with protocol requirements; 6. Sign informed consent. Children/adolescent subjects must obtain the informed consent of their legal guardians and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Currently in acute metabolic disorders, such as diabetic ketoacidosis, hypertonic hyperglycemia, etc.; 2. Women who are breastfeeding, pregnant or who ask to become pregnant during the trial; Have received immunosuppressive or regulatory drug therapy within the past 3.1 years; 4. Associated with other autoimmune diseases, such as systemic lupus erythematosus; 5. Severe diseases of liver, kidney, gastrointestinal tract, blood system, brain and circulatory system; 6. The woman is pregnant, breastfeeding or plans to become pregnant within 6 months; 7. Mental and nervous system diseases do not cooperate or do not take medicine on time, abuse drugs or other substances; Malignant tumor; 8. 9. Known hypersensitivity or allergic reaction to Lactobacillus paracasei or its excipients; 10. Surgery or stress; 11. The investigator judges that there is clear evidence of severe, active, uncontrolled endocrine or autoimmune abnormalities in the patient; 12. Is participating in another clinical trial.

Design outcomes

Primary

MeasureTime frame
Serum C-peptide;

Secondary

MeasureTime frame
HbA1C;The dosage of basic diabetes drug;Self-glucose monitoring;Islet autoantibodies;Lymphocyte subsets in peripheral blood;Cytokines level;C-reactive protein;

Countries

China

Contacts

Public ContactYu Liu

Sir Run Run Hospital, Nanjing Medical University

drliuyu@njmu.edu.cn+86 25 8711 5663

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026