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The Effect of Liposome Vitamin C on the Absorption and Metabolism of the Human Body.

The Effect of Liposome Vitamin C on the Absorption

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04886752
Enrollment
11
Registered
2021-05-14
Start date
2019-06-10
Completion date
2020-12-31
Last updated
2021-05-14

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

Conditions

Vitamin C Deficiency

Brief summary

To evaluate the difference between vitamin C in the form of oral liposomes and general vitamin C in a fixed period of time in plasma and urine.

Detailed description

we recruited 11 healthy subjects and adopted a cross-over test. the subjects need to take 3 tests during trail. After each test was completed, a washout period of 14 days was required before the next test start. The subjects were informed to consume one sachet vitamin C without liposome, liposomal process A vitamin C, or liposomal process B vitamin C (Double Nutri™) every test, and vitamin C concentration was measured at baseline (0 hours), 0.5, 1, 2, 3, 4, and 8 hours after taking test sample.

Interventions

DIETARY_SUPPLEMENTvitamin C without liposome

subjects need to take 3 tests during trail. After each test was completed, a washout period of 14 days was required before the next test start

DIETARY_SUPPLEMENTliposomal process A vitamin C

subjects need to take 3 tests during trail. After each test was completed, a washout period of 14 days was required before the next test start

DIETARY_SUPPLEMENTliposomal process B vitamin C (Double Nutri™)

subjects need to take 3 tests during trail. After each test was completed, a washout period of 14 days was required before the next test start

Sponsors

TCI Co., Ltd.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

1. Adults between 20-60 years old, 2. No heart, liver, kidney, endocrine and major organic diseases

Exclusion criteria

1. Renal insufficiency and dialysis 2. Cancer 3. Underweight (BMI≦17) or obese (BMI≧27), 4. Take chronic disease drugs, 5. Blood pressure systolic blood pressure ≧130 mmHg or diastolic blood pressure ≧85 mmHg, 6. Too high fasting blood glucose ≧ 100 mg/dL, 7. Triglyceride ≧ 150 mg/dL,Total cholesterol ≧ 200 mg/dL, 8. Have a history of vitamin C allergy, 9. People with mental illness, 10. Pregnant or breastfeeding women, 11. Hematosis, 12. Kidney stones, 13. Long-term vitamin C supplements (at least 200 mg per day for more than one month)

Design outcomes

Primary

MeasureTime frameDescription
vitamin c detectionat 8 hours after taking test samplevitamin c was assessed by Ascorbic Acid Colorimetric Assay Kit II
The change of Triglycerideat 8 hours after taking test sampleVenous blood was sampled to measure concentrations of Triglyceride
The change of body mass index (BMI)Time 0, 0.5, 1, 2, 3, 4, and 8 hours after taking test sampleBMI is a measurement of a person's leanness or corpulence based on their height and weight, and is intended to quantify tissue mass.The body mass index (BMI, kg/m\^2) and body mass (kg) were assessed by InBody770.
The change of aspartate aminotransferaseat 8 hours after taking test sampleVenous blood was sampled to measure concentrations of aspartate aminotransferase
The change of alanine aminotransferaseat 8 hours after taking test sampleVenous blood was sampled to measure concentrations of alanine aminotransferase
The change of creatineat 8 hours after taking test sampleVenous blood was sampled to measure concentrations of creatine

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026