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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06440486
Other study ID # WK2024008
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 15, 2024
Est. completion date December 15, 2024

Study information

Verified date May 2024
Source Wecare Probiotics Co., Ltd.
Contact Kang Liu, Doctor
Phone 15808432375
Email liukang@nsmc.edu.cn
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This clinical study aims to explore the effects of probiotics on inflammatory and metabolic indicators in patients with type 2 diabetes. By assessing the potential of probiotics to modify these markers, the study seeks to identify an economical and effective strategy for the prevention and treatment of type 2 diabetes.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 80
Est. completion date December 15, 2024
Est. primary completion date September 15, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: 1. Signed an informed consent form before the study and has a thorough understanding of the content, process, and possible adverse reactions of the study; 2. Age 18 (inclusive) and above, gender not limited; 3. Diagnosed with type 2 diabetes mellitus; 4. Not diagnosed with cardiovascular, kidney, or any other diabetic complications. Exclusion Criteria: 1. Age over 75 years old; 2. Use of exogenous insulin or patients with cardiovascular disease and other complications; 3. Patients who are currently using a-glucosidase inhibitors; 4. Patients who have a habit of taking probiotics or are currently taking probiotics; 5. Pregnant or lactating women; 6. Subjects deemed unsuitable for participation in this clinical study by the investigators due to other reasons.

Study Design


Intervention

Dietary Supplement:
Probiotics
Serum and fecal samples were collected at the beginning and end of the study to evaluate the effects of probiotic consumption on immune markers, metabolites, and gut microbiota before and after administration.

Locations

Country Name City State
China Nanchong Central Hospital Nanchong Sichuan

Sponsors (1)

Lead Sponsor Collaborator
Wecare Probiotics Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Inflammatory markers Blood samples will be collected from patients with type 2 diabetes mellitus (T2DM), centrifuged to obtain serum, and analyzed for tumor necrosis factor-alpha (TNF-a), interleukins 6 (IL-6), 10 (IL-10), and 18 (IL-18), IL-1ß, and interferon-gamma (IFN-?) to assess the impact of probiotics on T2DM patients. 12 weeks
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