Actively Recruiting
Efficacy and Safety of Sanggua Tablets in the Treatment of Patients With Impaired Glucose Tolerance and Mild Type 2 Diabetes
Led by Tongji Hospital · Updated on 2025-05-20
84
Participants Needed
1
Research Sites
135 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Type 2 diabetes mellitus (T2DM) and impaired glucose tolerance (IGT) are growing public health challenges. Early intervention in mild T2DM and IGT is essential to prevent disease progression and severe complications. Traditional Chinese Medicine (TCM) provides a potential therapeutic approach. Sanggua tablets, a TCM formula composed of mulberry leaf, bitter melon, kudzu root, Chinese yam, and cassia seed, embody TCM principles of clearing heat, generating body fluids, tonifying the spleen and stomach, and nourishing the lungs and kidneys. Modern studies show that Sanggua tablets effectively lower blood glucose and improve lipid profiles through components like mulberry polysaccharides and bitter melon saponins. These findings suggest their potential as an alternative or complementary therapy for mild T2DM and IGT. This study will conduct a randomized, double-blind, placebo-controlled, parallel-group clinical trial among patients with IGT and mild T2DM. Participants will receive a 16-week intervention with Sanggua tablets. The primary outcome is glycated hemoglobin (HbA1c), with secondary outcomes such as fasting blood glucose (FBG), fasting insulin (FINS), HOMA-IR, lipid profiles and so on. Safety will be closely monitored. Additionally, fecal samples will be collected for 16S rDNA sequencing to explore the role of gut microbiota in the therapeutic effects of Sanggua tablets. This study aims to provide evidence for the clinical application and development of Sanggua tablets as a novel TCM therapy.
CONDITIONS
Official Title
Efficacy and Safety of Sanggua Tablets in the Treatment of Patients With Impaired Glucose Tolerance and Mild Type 2 Diabetes
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18 to 70 with impaired glucose tolerance (IGT)
- Patients aged 18 to 70 with mild type 2 diabetes mellitus (T2DM) not requiring medication
- Glycated hemoglobin (HbA1c) between 5.6% and 7.5%
- Voluntarily sign informed consent and agree to follow study procedures
You will not qualify if you...
- Type 1 diabetes mellitus
- Allergy to Sanggua tablets or any ingredient
- Use of blood sugar or lipid-lowering drugs within 3 months
- Severe respiratory, cardiovascular, liver, kidney, rheumatic, or blood diseases
- Uncontrolled or unstable conditions like infections or electrolyte imbalances
- Kidney diseases, hypertension, heart failure, acidosis, or urinary infections causing protein in urine
- Psychiatric disorders
- Pregnant, planning pregnancy, or breastfeeding
- Long-term steroid therapy
- Poorly controlled or secondary hypertension
- Participation in other clinical trials within 3 months
- Any condition deemed by investigators as unsafe or interfering with the study
AI-Screening
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Trial Site Locations
Total: 1 location
1
Tongji Hospital
Wuhan, Hubei, China, 430030
Actively Recruiting
Research Team
G
Gang Yuan, Professor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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