Vitamin D - Clinical Trials
Posted: Wed Feb 10, 2016 8:06 am
Vitamin D and MS - Clinical Trials
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AntonioBR wrote:-The Standard Dose
Dr. Coimbra and Dr. Michael Holick found that 1,000 IU of Vitamin D3 per kilogram (or 500 IU per pound) is a good standard dose for people with autoimmune disease. They should take it every day. And if the person is obese "maybe" he/she should take more Vitamin D3. Because fat cells can steal vitamin D from your bloodstream. Dr. Michael Holick has a study and an interview about it.
The initial dose they recommend is: 1,000 IU D3/Kg. So, if a person weight 100kg (220.46 pounds) he/she should take 100,000IU Vit. D3 per day.
Which is 10000iu/dayAntonioBR wrote:Jan-Markus Dörr, Charite University, Berlin, Germany
Efficacy of Vitamin D Supplementation in Multiple Sclerosis (EVIDIMS)
Dose: 20 000 IU/2d 400/2d of vitamin D3 versus 400/2d, for 18 months
A paper regarding the trial (does not contain the actual results) also statesAntonioBR wrote:Preventing the risk of Multiple Sclerosis using Vitamin D in patients with a first demyelinating event in Australia and New Zealand (PrevANZ)
Dose: Vitamin D3 1 000 IU/d, 5 000 IU/d, 10 000 IU/d or placebo, for 48 weeks
The implication of the last sentence quoted above is that the researchers think a lower dose (than 10000IU) may be sufficient and that a higher dose would not help if the 10000IU does not help...document link here...Another important question relates to the dose used in the high-dose arm. In fact, we do not know, at which minimum doses or serum levels vitamin D starts to have immunomodulatory effects. To prevent failure of the trial because of an insufficient treatment dose, we choose the maximum dose for which sufficient safety data are available, which currently corresponds to 10.000 IU per day [23]. It might well be that already smaller doses would be sufficient, but on the other hand it is rather unlikely, that if this dose does not demonstrate any treatment effect, even higher daily doses would do
I agree with you more is not always better. Coimbra's Protocol doesn't have a dose of 60,000IU/D3 or higher. In fact, there are people that take half of this dose.Coimbra protocol is a dose of the order of say 60000IU+ whereas the first study is 10000IU and the second is only 1000IU to a max of 10000IU. The step up to 6+ times the dose could be very significant.
On this thread, I want to post all the clinical trials related to Vitamin D and MS. Even if goes against Coimbra's Protocol. I'm not aiming at defending this protocol at every cost. If possible, I want to discover the best treatment to MSThe above quoted trials are NOT "Coimbra Protocol" and cannot be used as evidence for such.
Without results these are nothing. However, by posting these without results will have people assume the outcomes were positive, which is misleading. Is that what you want?AntonioBR wrote:On this thread, I want to post all the clinical trials related to Vitamin D and MS. Even if goes against Coimbra's Protocol. I'm not aiming at defending this protocol at every cost.
If this statement is truly the case, what other treatments have you investigated? And what criteria do you use to validate their true effectiveness?If possible, I want to discover the best treatment to MS
Scientific studies are a 'must'. But think that +12,000 people are misleading themselves it's very unlikely. Overall, the average placebo effect is 33%.CureOrBust wrote:Without results these are nothing. However, by posting these without results will have people assume the outcomes were positive, which is misleading. Is that what you want?
I'm reading about LDN and Biotin.If this statement is truly the case, what other treatments have you investigated? And what criteria do you use to validate their true effectiveness?
So, there is a financial problem related.Conducting research is an expensive endeavor. Seed funds to help collect a small amount of pilot data, like Dr. Wahls’ current study, range from $75,000 to $100,000. A somewhat larger study testing the safety and tolerability of a study will cost $250,000 to $500,000. A clinical trial that is large enough to prove that the intervention is effective often costs a million dollars or more. Dr. Wahls has sent multiple grant proposals for $450,000 to the National MS Society and the National Institutes of Health (NIH), but has thus far has not been funded.
Without actual results, you will never know.AntonioBR wrote:But think that +12,000 people are misleading themselves it's very unlikely