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Evaluation of diglycerides in edible oil for lowering blood lipids, uric acid and weight loss

Evaluation of diglycerides in edible oil for lowering blood lipids, uric acid and weight loss

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083139
Enrollment
Unknown
Registered
2024-04-16
Start date
2024-04-16
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Hyperuricemia

Interventions

Diglyceride oil intervention group:Replace the oil from the stir-fry with the product provided - 80% diglyceride cooking oil

Sponsors

Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 50 Years

Inclusion criteria

Inclusion criteria: (1) 25 years old= age = 50 years old, male-to-female ratio: 2:1, BMI>18kg/m² (excluding thin people); (2) meet the diagnostic criteria for asymptomatic hyperuricemia; Asymptomatic hyperuricemia refers to patients with only hyperuricemia (blood uric acid = 450-540 µmol/L), or (blood uric acid = 450-480 µmol/L) combined with hypertension, dyslipidemia, diabetes, obesity, stroke, coronary heart disease, cardiac insufficiency, uric acid nephrolithiasis, renal impairment (= CKD2 stage), etc., but no clinical symptoms such as arthritis, tophi, uric acid stones, etc. (3) Good diet, no daily smoking (passive or active smoking no more than 1 hour a day), no alcohol (less than 14 times a week), no heavy dieting; (4) Ensure that other drugs that affect metabolism are not consumed during this experiment. Eat at home at least 5 times a week, and consume 25g of cooking oil per day; (5) Be able to comply with the requirements of clinical trials; (6) The subject or guardian has signed the informed consent form; (7) The patient fills in the written informed consent form and the food frequency questionnaire and undertakes to cooperate with the study throughout the trial period.

Exclusion criteria

Exclusion criteria: Those who have the following conditions will not be selected: (1) No long-term use of drugs related to lipid metabolism in the past 6 months; (2) Abuse of narcotics, psychotropic substances and cigarettes in the past 6 months; (3) Supplement nutrients, such as probiotics, multi-minerals, multivitamins, etc., at least twice a week during the study period or in the past 2 months; (4) rapid weight loss in the past 6 months, total parenteral nutrition and protein malnutrition; (5) Pregnant or lactating women, or those who plan to become pregnant in the next 6 months; (6) poor compliance and poor follow-up possibility;

Design outcomes

Primary

MeasureTime frame
Serum uric acid;

Secondary

MeasureTime frame
height;weight;waistline; blood routine examination;Blood pressure;Fasting blood glucose;Insulin levels;Glycosylated hemoglobin;Triglycerides;Total cholesterol;HDL cholesterol;LDL cholesterol;Serum HDL;Serum low-density lipoprotein;C-reactive protein;Serum creatinine;

Countries

China

Contacts

Public ContactYuanyuan Yan

Shanghai Jiao Tong University School of Medicine

yanyuanyuan0801@outlook.com+86 183 2197 0015

Outcome results

None listed

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