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Fecal Microbiota Transplantation for Type 2 Diabetes Mellitus and Hashimoto's Thyroiditis

Efficacy of Fecal Microbiota Transplantation in Improving Metabolic Parameters and Immune Dysregulation in Patients With Concurrent Type 2 Diabetes Mellitus and Autoimmune Thyroid Disease.

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07733232
Enrollment
38
Registered
2026-07-29
Start date
2026-08-01
Completion date
2027-12-01
Last updated
2026-07-29

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

Conditions

Autoimmune Thyroid Disease, FMT, Type 2 Diabetes Mellitus (T2DM)

Brief summary

The goal of this clinical trial is to learn if fecal microbiota transplantation (FMT) can improve metabolic control and immune function in adults with both type 2 diabetes and Hashimoto's thyroiditis (an autoimmune thyroid disease). It will also learn about the safety of FMT in these patients. The main questions it aims to answer are: Can FMT lower blood sugar levels (HbA1c, fasting blood glucose, and 2-hour post-meal blood glucose) in participants with type 2 diabetes? Can FMT reduce thyroid autoantibody levels (TPOAb and TgAb) in participants with Hashimoto's thyroiditis? This is a single-arm study, meaning all participants will receive the same FMT treatment. Researchers will compare each participant's results before and after the intervention to see if FMT has an effect. Participants will: Complete baseline tests including blood work and stool sample collection during the 2-week screening period Take 40 oral FMT capsules by mouth over about 1.5 hours under medical supervision at the start of the study Keep taking their usual diabetes and thyroid medications at the same dose throughout the study, unless their doctor says otherwise Return for follow-up visits and tests at 12 weeks and 24 weeks after the FMT treatment

Interventions

BIOLOGICALFecal microbiota transplantation oral capsules

All subjects received a single standardized fecal microbiota transplantation (FMT) intervention at Week 0 under unified protocols. After fasting, each subject took 40 standardized fecal microbiota suspension capsules in divided doses within 1.5 hours (2-3 capsules each time, swallowed with warm water).

Sponsors

Shen Xujun
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Age ≥ 18 and ≤ 65 years old. 2. Diagnosed with type 2 diabetes mellitus (T2DM). 3. Positive for thyroid peroxidase antibody (TPOAb) and thyroglobulin antibody (TgAb); thyroid ultrasonography indicates diffuse thyroid lesions. 4. The regimens of hypoglycemic drugs and thyroid-related basic treatments (including drug types and dosages) have remained stable for at least 3 months before enrollment.

Exclusion criteria

1. Subjects who have used antibiotics, probiotics or prebiotics within 4 weeks prior to screening. 2. Patients complicated with severe gastrointestinal diseases (e.g., inflammatory bowel disease, active gastrointestinal bleeding). 3. Patients receiving specialized treatment for hyperthyroidism (Graves' disease) or with a history of thyroid malignancy. 4. Patients with severe immunosuppression (neutrophil count \< 1500/mm³, lymphocyte count \< 500/mm³). 5. Patients with active severe gastrointestinal bleeding, intestinal perforation, or severe intestinal barrier/mucosal injury. 6. Patients with intestinal mucosal injury of unknown etiology. 7. Patients diagnosed with fulminant colitis or toxic megacolon. 8. Patients with active extraintestinal infection requiring treatment with broad-spectrum antibiotics. 9. Severe malnutrition (body mass index \< 15 kg/m²) or severe hypoalbuminemia (serum albumin \< 25 g/L). 10. Congenital or acquired immunodeficiency diseases. 11. Patients who have recently received high-risk immunosuppressants or cytotoxic drugs (e.g., rituximab, doxorubicin), or medium-to-high dose glucocorticoids (e.g., prednisone \>= 20 mg per day for more than 4 consecutive weeks). 12. Patients complicated with other autoimmune diseases. 13. Patients with severe hepatic or renal insufficiency. 14. Patients with malignant tumors. 15. Patients with known allergy to capsule ingredients. 16. Pregnant or lactating females.

Design outcomes

Primary

MeasureTime frame
Glycated Hemoglobin(HbA1c)baseline,week 12,week 24
Fasting blood glucosebaseline,week12,week24
2-hour postprandial blood glucosebaseline,week12,week24
Thyroid Peroxidase Antibody(TPOAb)baseline,week12,week24
Thyroglobulin Antibody(TgAb)baseline,week12,week24

Secondary

MeasureTime frame
Recovery of characteristic gut microbiotabaseline,week 12,week 24
Triglyceridesbaseline,week12,week24
Total cholesterolbaseline,week12,week24
Uric acidbaseline,week12,week24
Fasting Insulinbaseline,week12,week24
Body weightbaseline,week12,week24

Contacts

CONTACTXu Jun Shen
sxjsandy@126.com+8615906675015
CONTACTLing Ling Zhang
+8619706851581

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 30, 2026