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NUTRITION: Natural Tocotrienol Against Ischemic Stroke Event

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala
Ingia / Ingia
Kiungo kimehifadhiwa kwenye clipboard
Hali
Wadhamini
Chandan K Sen
Washirika
Government of Malaysia

Maneno muhimu

Kikemikali

A natural form of vitamin E called tocotrienol (TCT), found in many common foods such as barley, decreases stroke size in animal models. Vitamin E has blood-thinning properties and lowers cholesterol, which make it a potential therapy for stroke prevention, though these effects are less well characterized for TCT. We plan to conduct two trials (I & IIA) to determine the effects of orally supplemented TCT on platelet function and cholesterol.

Maelezo

A natural form of vitamin E called tocotrienol (TCT), found in many common foods such as barley, decreases stroke size in animal models. Vitamin E has blood-thinning properties and lowers cholesterol, which make it a potential therapy for stroke prevention, though these effects are less well characterized for TCT. We plan to conduct two trials (I & IIA) to determine the effects of orally supplemented TCT on platelet function and cholesterol. Phase I subjects will be healthy volunteers, recruited by an advertisement. Phase IIA subjects will be hyperlipidemic (having high cholesterol), and will be referred to us by their Wound Care Center Physicians. Patients will be randomized to receive placebo pills, (400 or 800 mg) TCT pills, low-dose 81 mg aspirin (commonly used for secondary prevention of stroke), or TCT and aspirin together. Potential subjects for Phase-I who meet study criteria and agree to participate will be in the study for 6 months and have the following study related procedures, blood draw total 4 times, tape stripping (non-invasive procedure), BMI, and blood pressure measurement at each visit (every month). Participants in Phase-IIA will have blood drawn a total of 6 times, tape stripping, BMI and blood pressure measurement and participants will be in the study for 13 months.

Tarehe

Imethibitishwa Mwisho: 02/28/2018
Iliyowasilishwa Kwanza: 04/04/2012
Uandikishaji uliokadiriwa Uliwasilishwa: 04/12/2012
Iliyotumwa Kwanza: 04/16/2012
Sasisho la Mwisho Liliwasilishwa: 03/19/2018
Sasisho la Mwisho Lilichapishwa: 03/20/2018
Tarehe halisi ya kuanza kwa masomo: 02/29/2012
Tarehe ya Kukamilisha Msingi iliyokadiriwa: 10/31/2018
Tarehe ya Kukamilisha Utafiti: 11/30/2018

Hali au ugonjwa

Ischemic Stroke
Transient Ischemic Attack (TIA)

Uingiliaji / matibabu

Other: Vitamin E tocotrienol (TCT) capsules ; Low dose Aspirin

Other: Placebo vehicle control

Awamu

Awamu 1/Awamu 2

Vikundi vya Arm

MkonoUingiliaji / matibabu
Active Comparator: Healthy Volunteers
Healthy participants randomized into one of 6 groups that will take 4 capsules, twice a day of vitamin E tocotrienol (TCT) capsules ; Low Dose Aspirin or placebo capsule for 7 months.
Active Comparator: Hyperlipidemic
hyperlipidemic patients randomized into one of 6 groups that will take 4 capsules, twice a day of Vitamin E Tocotrienol (TCT) capsules; Low Dose Aspirin or placebo vehicle control capsule for 7 months.

Vigezo vya Kustahiki

Zama zinazostahiki Kujifunza 40 Years Kwa 40 Years
Jinsia Inastahiki KujifunzaAll
Hupokea Wajitolea wa AfyaNdio
Vigezo

Phase IA

Inclusion Criteria:

- Healthy subjects between 40 and 70 years of age

- No history of long-term vitamin E supplement (defined as daily oral tocopherol or tocotrienol supplementation greater than or equal to 6mos; within the past 5 years)

- No current vitamin E supplementation in multivitamin

Exclusion Criteria - (as self reported by potential participants during review of eligibility criteria with Research Nurse,)

- Evidence of heart disease as diagnosed by a physician by one or more of the following tests; EKG, chest x-ray, stress test, tilt table test, echocardiogram, coronary angiogram, electrophysiology test, CT heart scan, coronary MRI, pericardiocentesis

- High cholesterol (total cholesterol >240mg/dL, LDL>160mg/dL)

- Prior cancer diagnosis

- Pregnancy - To exclude the possibility of pregnant women entering the study or becoming pregnant during the study only post-menopausal women or women who have had hysterectomies or bilateral oophorectomies will be included.

- Breast feeding

- Smoker (Must have quit 5 or more years ago)

- Alcohol dependence (>4 drinks per day for more than 1yr anytime in the last 3 years)

- Medication exclusion criteria - current use or recent discontinuation (within last 28 days) of any medication including the following: anti-coagulants and blood-thinners (e.g., Warfarin), psychotropic medications including antipsychotics, mood-stabilizers (e.g., lithium, valproic acid, carbamazepine/tegretol); anti-depressants (tricyclics, SSRI's, MAOI's, nonselective MAOIs, Wellbutrin, St. John's Wort); anti-anxiety/anti-panic agents; anti-obsessive agents; prescription stimulants (e.g., Provigil, Ritalin); diet pills/anorectics; daily medication for chronic pain (e.g., opiates) or muscle spasms; daily use of over the counter stimulants in pill form (e.g., ephedrine); daily medication for asthma, Parkinson's disease medications (e.g., levodopa, methyldopa, apomorphine), smoking cessation medications (Wellbutrin/Zyban, Chantix/varenicline); statin use is not grounds for exclusion.

Phase IIA

Inclusion Criteria:

- Hyperlipidemic patients between 40 and 70 years of age currently taking statins

- LDL>130mg/dL

- TG>150mg/dL

- HDL<40mg/dL

- No history of long-term vitamin E supplement (defined as daily oral tocopherol or tocotrienol supplementation greater than or equal to 6mos; within the past 5 years)

- No current vitamin E supplementation in multivitamin

Exclusion Criteria:

- Evidence of heart disease as diagnosed by a physician by one or more of the following tests; EKG, chest x-ray, stress test, tilt table test, echocardiogram, coronary angiogram, electrophysiology test, CT heart scan, coronary MRI, pericardiocentesis

- Prior cancer diagnosis

- Currently taking blood thinners

- Pregnancy - To exclude the possibility of pregnant women entering the study or becoming pregnant during the study only post-menopausal women or women who have had hysterectomies or bilateral oophorectomy will be included.

- Breast feeding

- Smoking (Must have quit within the past 6 months)

- Alcohol dependence - (>4 drinks per day for more than 1yr anytime in the last 3 years)

- Medication exclusion criteria - current use or recent discontinuation (within last 28 days) of any medication including the following: anti-coagulants and blood-thinners (e.g., Warfarin), psychotropic medications including antipsychotics, mood-stabilizers (e.g., lithium, valproic acid, carbamazepine/tegretol); anti-depressants (tricyclics, SSRI's, MAOI's, nonselective MAOIs, Wellbutrin, St. John's Wort); anti-anxiety/anti-panic agents; anti-obsessive agents; prescription stimulants (e.g., Provigil, Ritalin); diet pills/anorectics; daily medication for chronic pain (e.g., opiates) or muscle spasms; daily use of over the counter stimulants in pill form (e.g., ephedrine); daily medication for asthma, Parkinson's disease medications (e.g., levodopa, methyldopa, apomorphine), smoking cessation medications (Wellbutrin/Zyban, Chantix/varenicline)

Matokeo

Hatua za Matokeo ya Msingi

1. Platelet function panel [up to one year]

Blood draw followed by platelet aggregometry

2. Lipid profile [up to one year]

blood lipid panel including HDL, LDL, total cholesterol

Hatua za Matokeo ya Sekondari

1. Tape Stripping Test [up to one year]

HPLC vitamin E analysis of tape strips for compliance

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