Skip to content

Study on The Intervention Effect on Patients with Dyslipidemia of Dampness Syndrome

Study on The Intervention Effect on Patients with Dyslipidemia of Dampness Syndrome

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006576
Enrollment
Unknown
Registered
2022-09-09
Start date
2022-09-16
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Dyslipidemia

Interventions

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.18-70 years old. 2.Those who meet the typical diagnosis of dampness syndrome in the Diagnostic Standard of Dampness Syndrome of Traditional Chinese Medicine V2.0. 3.Those who meet the diagnosis of dyslipidemia in the guidelines for Prevention and Treatment of Dyslipidemia in Chinese Adults (2016 revised Edition). 4.Patients whose cardiovascular risk assessment is medium risk and low risk. 5.Those who volunteer to participate in the study of this subject and sign informed consent forms.

Exclusion criteria

Exclusion criteria: 1. Patients with nephrotic syndrome, hypothyroidism, renal failure, liver disease, systemic lupus erythematosus, myeloma, glycogen accumulation, lipoatrophy, acute porphyria and polycystic ovary syndrome. 2. Patients who are using drugs related to blood lipid metabolism, such as diuretics, beta blockers, glucocorticoids, metformin, insulin, contraceptive. 3. Patients with systolic blood pressure = 180mmHg or diastolic blood pressure = 110mHg after treatment. 4. Patients whose fasting blood glucose was still = 11.1mmol/L after oral drug treatment. 5. Patients whose TG = 5.65mmol/L. 6. Patients with systemic severe diseases such as heart, liver, kidney, hematopoietic system, immune system, etc. 7. Pregnant or lactating women or people who plan to become pregnant during the trial or whose spouse plans to become pregnant. 8. Patients with allergic constitution, who may be allergic to this drug or who are mentally ill. 9. Other patients who can't cooperate for a long time.

Design outcomes

Primary

MeasureTime frame
Outcome: High density lipoprotein cholesterol (HDL-C);Cardiovascular risk assessment;Triglyceride (TG);Score of Dampness Syndrome Scale;Low density lipoprotein cholesterol (LDL-C);Total cholesterol (TC);

Secondary

MeasureTime frame
HbA1c;Fasting insulin;Interleukin-6;Body mass index (BMI);Insulin resistance index;C-reactive protein (CRP);Blood pressure;Tumor necrotic factor-a (TNF-a);Fasting plasma glucose;Intestinal flora;Uric acid (UA);Insulin action index;

Countries

China

Contacts

Public ContactChen Xinyan

Guangdong Provincial Hospital of Chinese Medicine

chenxinyancxy@163.com13539984767

Outcome results

None listed

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