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Effects of dietary flaxseed supplement formula on dyslipidemia

Effects of dietary flaxseed supplement formula on dyslipidemia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126058
Enrollment
Unknown
Registered
2026-06-03
Start date
2022-01-12
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

Hyperlipemia

Interventions

Flaxseed first followed by rice flour:Subjects in the flaxseed-first then rice flour group took flaxseed formula powder twice daily, 30 grams each time to replace staple foods in meals, with an 8-week
Rice flour first then flaxseed group:Subjects in the rice-flaxseed sequential group took rice flour twice daily, 38.5 g each time to replace staple foods in meals, with an intervention period of 8 wee

Sponsors

The Second Affiliated Hospital of Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Local permanent residents with no plan to move out within the next year, patients with dyslipidemia aged 18 years and above. 2. Normal body temperature and no pulmonary infection. 3. Subjects diagnosed with hyperlipidemia according to the Chinese Guidelines for the Prevention and Treatment of Adult Dyslipidemia (2016 Revised Edition), with triglyceride TG>= 1.70 mmol/L.

Exclusion criteria

Exclusion criteria: 1.Residents aged < 18 years. 2. Subjects taking medications that may affect the results, such as lipid-lowering drugs, appetite suppressants, long-term antibiotics, or taking health supplements that may influence lipid levels, such as fish oil. 3. Subjects with hyperlipidemia induced by medications, such as corticosteroids, ß-blockers, oral contraceptives, interferons, retinoic acid, diuretics. 4. Subjects diagnosed with familial lipoprotein lipase (LPL) deficiency, familial apolipoprotein C-II (ApoC-II) deficiency, familial type III or V hyperlipidemia. 5. Subjects with alcohol dependence or abuse. 6. Subjects with hypothyroidism, Cushing's syndrome, acromegaly, nephrotic syndrome, chronic renal failure, systemic lupus erythematosus, multiple myeloma, or non-alcoholic steatohepatitis (NASH). 7. Subjects allergic to flaxseed or consumed dietary flaxseed supplements in the past six months.

Design outcomes

Primary

MeasureTime frame
Triglycerides;

Secondary

MeasureTime frame
Total cholesterol;Low-density lipoprotein;High-density lipoprotein;Body Composition Analysis;

Countries

China

Contacts

Public ContactZhang Pianhong

The Second Affiliated Hospital of Zhejiang University School of Medicine

zrlcyyzx@zju.edu.cn+86 137 5711 9193

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026