Status:
UNKNOWN
Clinical Study on Wuling Powder in Treating Metabolic Syndrome of Spleen Deficiency and Dampness
Lead Sponsor:
Jiangsu Famous Medical Technology Co., Ltd.
Conditions:
Metabolic Syndrome
Eligibility:
All Genders
18-70 years
Phase:
PHASE4
Brief Summary
In this study, a randomized, partially double-blind, controlled, multi-center clinical research method was used. A total of 4 groups were designed, namely, single decoction group, co-decoction group, ...
Detailed Description
The research purpose of this project is to observe the effectiveness and safety of Wulingsan single decoction granules compared with traditional powder, co-decoction granules and analogues in the trea...
Eligibility Criteria
Inclusion
- Patients who meet the diagnostic criteria of metabolic syndrome;
- TCM syndrome differentiation of spleen deficiency and dampness patients;
- Patients with phlegm-dampness constitution score\>30;
- Patients aged 18 to 70 years;
- Patients who have signed informed consent and are highly compliant.
Exclusion
- Patients with hypertension, hyperglycemia, and hyperlipidemia caused by secondary metabolic syndrome (disease, drugs, surgery, etc.);
- Patients with severe primary diseases such as heart, liver, kidney, lung, brain, endocrine, hematopoietic system in the past or at the time of enrollment;
- Those who are confirmed to have acute coronary syndrome, malignant arrhythmia, and other serious heart diseases;
- Patients with co-infection, malignant tumors or mental illness;
- Patients with Cushing syndrome;
- Patients with allergies or allergies to this drug;
- Pregnant or breastfeeding women;
- Those who have adjusted hypoglycemic, lipid-lowering, antihypertensive drugs or taking weight-loss drugs within 1 month before enrollment.
Key Trial Info
Start Date :
April 1 2021
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
May 1 2023
Estimated Enrollment :
320 Patients enrolled
Trial Details
Trial ID
NCT04812236
Start Date
April 1 2021
End Date
May 1 2023
Last Update
March 23 2021
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