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Demonstration research on platform construction of intervention of phlegm and blood stasis by TCM internal and external treatment

Demonstration research on platform construction of intervention of phlegm and blood stasis by TCM internal and external treatment

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900025849
Enrollment
Unknown
Registered
2019-09-11
Start date
2018-09-01
Completion date
Unknown
Last updated
2019-09-16

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

Conditions

Dyslipidemia

Interventions

Sponsors

The Affiliated Hospital of Liaoning University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Non-spleen deficiency turbid non-hyperlipidemia group inclusion criteria: 1. Non-dyslipidemia: Adult fasting 12 hours serum TC 1.0 mmol/L (40 mg/dl); 2. TCM diagnosis did not reach the diagnostic criteria for spleen deficiency, phlegm and spleen deficiency syndrome; 3. Aged 18 to 75 years old; 4. Volunteer to participate in the trial and sign the informed consent form. Dyslipidemia patients enrolled in the standard1 Western medicine meets the diagnostic criteria for dyslipidemia: 1. Adult fasting 12 hours serum TC >=5.2mmol/L (200mg/dl) or TG >=1.7mmol/L (150mg/dl), or LDL-C >=3.4 mmol/L (130mg / dl Or HDL-C <1.0 mmol/L (40 mg/dl). TC is a mandatory item; 2. medical history for more than three months; 3. Chinese medicine meets the diagnostic criteria of spleen-qi deficiency syndrome or spleen deficiency and phlegm syndrome; 4. Aged 18 to 75 years old; 5. Volunteer to participate in the trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Subjects with acute myocardial infarction, cerebrovascular accident, severe trauma or major surgery within six months; 2. Secondary hyperlipidemia: Hyperlipidemia caused by nephrotic syndrome, hypothyroidism, gout, acute or chronic hepatobiliary diseases, and diabetes; 3. Family hereditary dyslipidemia; 4. Hyperlipidemia caused by drugs (phenothiazines, beta-blockers, adrenocortical steroids and certain contraceptives, etc.); 5. Heparin, thyroxine therapeutics, and other subjects who are affecting lipid metabolism drugs are being used; 6. Take antibiotics within 2 months before sampling, take microbial live bacteria preparations (including yogurt) within 1 week before sampling, and take statin lipid-lowering drugs 2 weeks before sampling; 7. Consolidation of subjects with severe primary diseases such as liver, kidney, and hematopoietic system.

Design outcomes

Primary

MeasureTime frame
Intestinal flora;Blood lipid;Intestinal flora pathway protein;

Secondary

MeasureTime frame
Lipid metabolism related protein;

Countries

China

Contacts

Public ContactMin Chen

The Affiliated Hospital of Liaoning University of Traditional Chinese Medicine

13704012000@163.com+86 13704012000

Outcome results

None listed

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