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Perilla seed oil as an adjunctive treatment with a statin improves lipid profiles in elderly: a post hoc data analysis.

Perilla seed oil as an adjunctive treatment with a statin improves lipid profiles in elderly: a post hoc data analysis.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20230913003
Enrollment
182
Registered
2023-09-13
Start date
2014-11-13
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Dyslipidemia in mild to moderate dementia patients. Perilla seed oil, Statin, Lipid level, Dementia

Interventions

received two capsules of perilla seed oil three times per day before a meal three grams per day,received two capsules of perilla seed oil three times per day before a meal three grams per day for two
a perilla seed oil and statin group ,a perilla seed oil group ,a statin group ,group without perilla seed oil and statin

Sponsors

Center of Excellence in Stroke, Thammasat University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 90 Years

Inclusion criteria

Inclusion criteria: The patients were 50-90 years old and gained 10-23 scores measured by the Thai Mental State Examination (TMSE) or 7-20 scores measured by the Thai Montreal Cognitive Assessment (MoCA-Thai). They suffered from mild to moderate dementia based on the Diagnosis and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV). They could recognize and communicate and gave written informed consent.

Exclusion criteria

Exclusion criteria: They were found to have creatinine greater than 2 mg/dL on the recruitment day. Their laboratory results showed 2.5 times greater abnormal liver function than the upper normal limit. The patients had treatable causes of dementia, such as vitamin B12 deficiency, hypothyroidism, normal pressure hydrocephalus, and neuro-syphilis. They had bleeding disorders. They were receiving warfarin or taking supplements. They suffered from major depression. They were allergic to medicinal and herbal medicines.

Design outcomes

Primary

MeasureTime frame
lipid profile Baseline, 3 month, and 6 month post-dose Low Density Lipoprotein ,lipid profile Baseline, 3 month, and 6 month post-dose High Density Lipoprotein,lipid profile Baseline, 3 month, and 6 month post-dose Triglyceride,lipid profile Baseline, 3 month, and 6 month post-dose Total cholesterol,lipid profile Baseline, 3 month, and 6 month post-dose Low Density Lipoprotein/High Density Lipoprotein ratio

Secondary

MeasureTime frame
Blood sugar Baseline, 3 month, and 6 month post-dose Fasting Blood Sugar,Blood sugar Baseline, 3 month, and 6 month post-dose Hemoglobin A1c ,Liver function levels Baseline, 3 month, and 6 month post-dose Serum glutamic oxaloacetic transaminase,Liver function levels Baseline, 3 month, and 6 month post-dose serum glutamic pyruvic transaminase,Renal function levels Baseline, 3 month, and 6 month post-dose Blood Urea Nitrogen,Renal function levels Baseline, 3 month, and 6 month post-dose Creatinine,Renal function levels Baseline, 3 month, and 6 month post-dose Glomerular Filtration Rate,complete blood count Baseline, 3 month, and 6 month post-dose White Blood Cell Count,complete blood count Baseline, 3 month, and 6 month post-dose Red blood cell ,complete blood count Baseline, 3 month, and 6 month post-dose Hematocrit,complete blood count Baseline, 3 month, and 6 month post-dose Neutrophil /Lymphocyte Platelet ratio

Countries

Thailand

Contacts

Public ContactRapeebhorn Chanapuk

Thummasat University Hospital

rapeeporncha@mcru.ac.th0636640966

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026