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Characteristics of changes in intestinal flora after therapy of liraglutide alone or combined with probiotics in T2DM patients

Characteristics of changes in intestinal flora after therapy of liraglutide alone or combined with probiotics in T2DM patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600118507
Enrollment
Unknown
Registered
2026-02-06
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-02-16

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

Conditions

T2DM

Interventions

Conventional comprehensive treatment group:None
Liraglutide treatment group:None
combined probiotics treatment group:None

Sponsors

Yunnan First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion Criteria 1. Meeting the diagnostic criteria for T2DM as specified in the *Guidelines for the Prevention and Treatment of Type 2 Diabetes in China (2020 Edition)*; 2. Having dyslipidemia (meeting the diagnostic criteria in the *Guidelines for the Prevention and Treatment of Adult Dyslipidemia in China (2016 Revised Edition)*, i.e., total cholesterol >= 5.18 mmol/L, or triglycerides >= 1.69 mmol/L, or low-density lipoprotein cholesterol >= 3.39 mmol/L, or high-density lipoprotein cholesterol = 20 years; 4. Having complete clinical data, with accessible baseline and follow-up data on diagnosis and treatment for at least 6 months; 5. The patient or their family members having signed an informed consent form for the use of data in this study (re-authorization for the use of retrospective data).

Exclusion criteria

Exclusion criteria: Exclusion criteria 1. Patients with combined severe dysfunction or advanced lesions of heart, brain, liver, kidney and other organs (such as heart failure with NYHA class ?-?, decompensated cirrhosis, renal failure requiring dialysis, etc.); 2. Patients with other severe metabolic diseases (such as Cushing's syndrome, acromegaly, etc.) or autoimmune diseases; 3. Patients with a history of mental illness or cognitive impairment who cannot cooperate with routine diagnosis and treatment; 4. Patients who have long-term used drugs that may significantly affect the activity of probiotics or intestinal flora (such as broad-spectrum antibiotics, bismuth agents, etc.) during the observation period, and whose impact cannot be evaluated; 5. Patients with severely missing clinical data that cannot be used for statistical analysis; 6. Patients with other diseases that may affect metabolism or intestinal flora, such as malignant tumors and acute stage of infectious diseases.

Design outcomes

Primary

MeasureTime frame
gut microbiota;

Countries

China

Contacts

Public ContactXu Ning

Yunnan First People's Hospital

xuning_0629@yeah.net+86 133 0871 1366

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026