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Clinical Efficacy and Mechanism of Gegaoqinliantang in Treating Obese/Overweight Type 2 Diabetes Patients with Damp-Heat Syndrome

Clinical Efficacy and Mechanism of Gegaoqinliantang in Treating Obese/Overweight Type 2 Diabetes Patients with Damp-Heat Syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000462
Enrollment
Unknown
Registered
2024-09-21
Start date
2024-05-01
Completion date
Unknown
Last updated
2024-10-14

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

Experimental group:At the same time of basic treatment of diabetes modified Gegenqinlian decoction combined with adequate metformin tablets was given
Control group:At the same time of basic treatment of diabetes adequate metformin tablets were given

Sponsors

Chengdu Shuangliu District Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) aged between 18 and 70 years old (2) patients with type 2 diabetes who met the diagnostic and classification criteria of diabetes (3) body mass index over 24.0kg/m2 (4) Poor glycemic control after lifestyle intervention {7.0%= glycosylated hemoglobin =9.0% and fasting blood glucose (FBG) =11.1mmol/L} (5) those who voluntarily participated in the study and signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) patients with type 1 diabetes; Patients with latent autoimmune diabetes in adults malignant tumors or other autoimmune diseases (2) patients with gastrointestinal and/or periodontal diseases; (3) acute diabetic complications including diabetic ketoacidosis diabetic hyperosmolar nonketotic coma hypoglycemic coma or severe unconscious hypoglycemia; (4) patients with heart failure unstable angina pectoris severe arrhythmia and myocardial infarction in the past 12 months; Blood pressure SBP > 180mmHg or DBP > 100mmHg; (5) history of liver disease such as cirrhosis hepatitis B or C (except carriers) or AST or ALT higher than 2.5 times the upper limit of normal; (6) history of renal disease or clinical diagnosis of renal insufficiency serum creatinine > 1.5mg/dl (132.6µmol/L); (7) patients with other endocrine system diseases such as hyperthyroidism hypercortisonism etc.; (8) those who are suffering from severe trauma severe infection or undergoing surgery and those who have received treatment but have not fully recovered; (9) patients with mental disorders drug or other substance abuse or alcoholism; (10) patients receiving steroid therapy or receiving treatment for malignant tumors; (11) Allergic constitution or allergic to the drugs used in the study; (12) pregnant lactating women women of childbearing age who have not taken effective contraceptive measures or plan to become pregnant during the trial and the urine HCG test result is positive;

Design outcomes

Primary

MeasureTime frame
diamine oxidase;The autophagy-related protein Atg7;HbA1c;blood fat;Serum lipopolysaccharide;Blood sugar;Neutrophil gelatinase-associated lipocalin;insulin release test;D-lactic acid;standard glucose tolerance test;

Secondary

MeasureTime frame
Satiety index;HOMA islet ß cell function index;insulin sensitivity index;TCM syndrome score;HOMA insulin resistance index;

Countries

CHINA

Contacts

Public ContactFANG WEI

Chengdu Shuangliu District Hospital of Traditional Chinese Medicine

fangw139@163.com+86 139 0804 6743

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026