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Effects of Ramulus Mori (Sangzhi) Alkaloids Tablets on Body Composition, Visceral Fat, and Related Metabolic Parameters in Patients with Type 2 Diabetes Mellitus

Effects of Ramulus Mori (Sangzhi) Alkaloids Tablets on Body Composition, Visceral Fat, and Related Metabolic Parameters in Patients with Type 2 Diabetes Mellitus

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600122172
Enrollment
Unknown
Registered
2026-04-09
Start date
2026-04-09
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Type 2 diabetes mellitus

Interventions

Ramulus Mori (Sangzhi) alkaloids (SZ-A) group:None
Acarbose group:None

Sponsors

Hunan University of Medicine General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients who visited the endocrinology outpatient or inpatient department at Hunan University of Medicine General Hospital from January 2023 to December 2025, and were diagnosed with type 2 diabetes (according to the 1999 WHO criteria); 2. Aged 18–80 years, any gender; 3. Records of body composition/visceral fat measurements (using the same model equipment) available at baseline and 24 weeks (+/- weeks) after medication; 4. Mulberry branch total alkaloid group: continuously used mulberry branch total alkaloid tablets (50 mg three times daily) for >=24 weeks, with complete records before and after medication; Acarbose group: continuously used acarbose tablets (50 mg three times daily) for >=24 weeks; both groups may be combined with metformin (stable dose), and may be combined with other non-a-glucosidase inhibitor hypoglycemic drugs (stable for >=12 weeks); 5. Complete medical records, including key indicators required for the study (HbA1c, blood lipids, uric acid, etc.).

Exclusion criteria

Exclusion criteria: 1. Type 1 diabetes, gestational diabetes, or other specific types of diabetes; 2. Switched a-glucosidase inhibitors during medication (e.g., from acarbose to SZ-A, or vice versa), or poor medication compliance (explicitly documented discontinuation or switching in medical records); 3. Complicated with severe heart, liver, or kidney dysfunction (NYHA class III/IV, ALT/AST > 2.5×ULN, eGFR < 60 ml/min), malignant tumors, or major surgery or trauma; 4. Pregnant or breastfeeding women; 5. Currently using weight-affecting drugs such as weight-loss medications or systemic corticosteroids; 6. Key data missing (e.g., baseline VFA or 24-week VFA missing).

Design outcomes

Primary

MeasureTime frame
Visceral fat area ;

Secondary

MeasureTime frame
Body composition parameters (skeletal muscle mass, body fat percentage, subcutaneous fat area);General data and endocrine and metabolic-related indicators;

Countries

China

Contacts

Public ContactShaolin Peng

Hunan University of Medicine General Hospital

pengsl90@163.com+86 745 238 3719

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026