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临床试验/NCT00678834
NCT00678834已完成1 期

Human Tissue Distribution of Orally Supplemented Natural Vitamin E Tocotrienol

Chandan K Sen1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2006年3月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
80
试验地点
1
主要终点
The Levels of TCT in the Tissues of "Non-healthy" Subjects and in the Tissue of "Healthy" Subjects Following Oral Supplementation (200 mg x 2 Per Day for 4-24 Weeks)

研究概览

简要总结

Levels of tocotrienol in human tissues following supplementation is not currently known. The objective of this present study is to determine the levels of this form of vitamin E in the human tissues such as skin, heart, lung, liver, adipose tissue, Brain and cerebrospinal fluid (CSF) following oral supplementation

详细描述

In nature, there are eight members in the vitamin E family: a-, b-, g- and d-TCP, and a-, b-, g- and d-tocotrienol (TCT). Vitamin E research has developed highly asymmetrically. Out of the 25,000+ papers on vitamin E in the PubMed, 99% deal with tocopherols. Recent research has demonstrated the lack of cancer-preventive effects and potential adverse health consequences of tocopherol (6). As a result, more attention has been turned towards non-tocopherol forms of vitamin E (16). Palm oil represents a major source of natural TCT. TCT possess powerful neuroprotective, antioxidant, anti-cancer and cholesterol lowering properties that often differ from the properties of TCP (15).

During the last five years, our and other laboratories have reported several striking beneficial properties of tocotrienols in experimental settings. One major concern that limits enthusiasm for tocotrienol for humans is the report that the vitamin E transporting protein, tocopherol-transport protein (TTP), has a very low affinity to transport tocotrienol. Using TTP-knock out mice, we have recently demonstrated that oral TCT is effectively carried to vital organs and that such transport can take place independent of TTP. With that background, the purpose of this project is to test the hypothesis that orally supplemented tocotrienol reaches the vital organs of humans.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
Single (Participant)

入排标准

年龄范围
21 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Aim 1 Surgical candidate with a surgery schedule date with a time period of 4-24 weeks (<4 weeks will be excluded; last dose until 24h before surgery) In Aim 1 we expect to have patients, with diverse co-morbidity and medication conditions.
  • •Patient Selection: Because of limitation in obtaining healthy human tissues (as in Aim 2), we plan to obtain these tissues from patients who are scheduled for the following surgeries for subjects in group one:
  • •Heart Heart Transplant Heart Failure- Biopsy taken from diseased heart Lung Lung Transplant, Lung-wedge/resection, Lobectomy Cancer- Tissue sample taken from removed lung or resected portion of lung Liver Liver Transplant, Biopsy, Resection Hepatic Malignancy- Biopsy taken from resected portion of liver Adipose Tissue Panniculectomy Excessive Tissue of the Abdomen Brain & CSF Epilepsy Excised brain tissue and cerebrospinal fluid
  • •To ensure higher enrollment we are not controlling for age of subjects as long as the subjects are 21 years of age or older.
  • •Inclusion Criteria Aim 1:
  • •age 21 and older
  • •good health
  • •non- smoker
  • •no current medications
  • •non- pregnant or non-breastfeeding
  • •no previous use of OTC medications or other form of supplements containing vitamin-E.
  • •Inclusion Criteria Aim 2:
  • •age 21 - 40 years
  • •good health
  • •non- smoker
  • •no current medications
  • •non- pregnant or non-breastfeeding
  • •no previous use of OTC medications or other form of supplements containing vitamin-E.

排除标准

  • •Long-term use of OTC medications containing vitamin-E or current vitamin-E supplements
  • •Scheduled surgery date lesser than 4 weeks or greater than 24 weeks.
  • •Exclusion Criteria Aim 2:
  • •Over 40 or under 21 years of age
  • •Current smoker
  • •Pregnant and breastfeeding
  • •Diabetes and HIV diagnosis
  • •Immunosuppression therapy
  • •Any neurological problems
  • •Long-term use of OTC medications containing vitamin-E or current vitamin-E supplements
  • •ETOH or drug abuse

研究组 & 干预措施

Arm 1

Active Comparator

To surgery patients, Tocotrienol capsules. 200mg (2 100mg capsules) to take by mouth twice daily to total 400mg daily

干预措施: To surgery patients, Tocotrienol capsules. (Dietary Supplement)

Arm 2

Active Comparator

To surgery patients, Tocopherol capsules. 200mg (2 100mg capsules) to take by mouth twice daily to total 400mg daily

干预措施: To surgery patients, Tocopherol capsules. (Dietary Supplement)

Arm 3

Active Comparator

Tocotrienol to healthy subjects - 200 mg to take orally two times a day (400 mg a day).

干预措施: Tocotrienol to healthy subjects. (Dietary Supplement)

结局指标

主要结局

The Levels of TCT in the Tissues of "Non-healthy" Subjects and in the Tissue of "Healthy" Subjects Following Oral Supplementation (200 mg x 2 Per Day for 4-24 Weeks)

时间窗: After at least 1 month of supplementation

次要结局

未报告次要终点

研究者

发起方
Chandan K Sen
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Chandan K Sen

Professor

Ohio State University

研究点 (1)

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