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STUDY ON THE MECHANISM OF HUANGLIAN WENDAN DECOCTION IN TREATING METABOLIC SYNDROME BASED ON LC-MS SERUM METABOLOMICS

STUDY ON THE MECHANISM OF HUANGLIAN WENDAN DECOCTION IN TREATING METABOLIC SYNDROME BASED ON LC-MS SERUM METABOLOMICS

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069296
Enrollment
Unknown
Registered
2023-03-13
Start date
2021-07-01
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

metabolic syndrome (MS)

Interventions

Treatment group:Conventional western medicine treatment + Huanglian Wendan decoction
Control group:Conventional western medicine treatment
Health group:None

Sponsors

The First Affiliated Hospital of Heilongjiang University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. No gender limit, aged between 30 and 75 years. 2. In line with the Western diagnostic standards for MS and the TCM phlegm-heat stasis syndrome differentiation standards, and in line with the medication plan. 3. Fully understand the nature, purpose and content of the clinical trial, participate voluntarily, and sign the informed consent. 4. Previous treatment with other traditional Chinese medicine, after 1 month washout period.

Exclusion criteria

Exclusion criteria: 1. Patients with malignant tumors, organ failure, transplantation and other serious chronic diseases. 2. Long-term use of thyroid medications, steroids and estrogen. 3. Patients with uncontrolled hypertension (SBP>=180 and/or DBP>=110), severe cardiopulmonary insufficiency, severe arrhythmias (rapid atrial fibrillation, atrial flutter, paroxysmal ventricular tachycardia, etc., sinus arrest, sinus bradycardia, sick sinus syndrome, complete bundle branch block), and the acute phase of other serious diseases. 4. Severely infected persons who have not been effectively controlled. 5. Patients with uncontrolled hyperglycemia and severe complications of diabetes. 6. Familial refractory hyperlipidemia. 7. Patients with abnormal liver function (ALT/AST > 1.5 times of normal value), abnormal kidney function (Cr > 1.5 times of normal value), severe damage to hematopoietic and autoimmune systems. 8. Pregnant and lactating patients and those who have fertility requirements within 3 months. 9. Patients with disabilities defined by law who are blind, deaf, mute, physically disabled, mentally retarded, or unable to express subjective symptoms of discomfort. 10. Suspected or confirmed history of alcohol and drug abuse. 11. Patients who are allergic, or allergic to more than three kinds of food or drugs. 12. Patients who have participated in clinical studies of other drugs or are using other traditional Chinese medicine products within the last 1 month. 13. Patients unable to receive regular follow-up. 14. Any other factors affecting test results and data acquisition and accuracy.

Design outcomes

Primary

MeasureTime frame
Blood pressure (systolic and diastolic);Blood fat (high-density lipoprotein, triglyceride);Fasting blood-glucose;Waistline;

Secondary

MeasureTime frame
Traditional Chinese medicine syndrome score;

Countries

China

Contacts

Public ContactTang Yue (tutor: Liu Li)

The First Affiliated Hospital of Heilongjiang University of Chinese Medicine

467748847@qq.com+86 188 4676 1162

Outcome results

None listed

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