jill
New Member
Posts: 1
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Post by jill on Mar 16, 2012 19:16:10 GMT -5
I recently participated in a study with about 18 blood draws per weekend (of 3) and had an average of 4 resticks each weekend. A week after completion I received a call from the coordinater who stated that because of the high number of resticks and for "the sake of the integrity of future studies", I would now be restricted from participating in studies with more than 10 draws per dose!!! Has anyone else had an experience like this?? New policy? How do I have this restriciton lifted?
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Post by sam9009 on Mar 20, 2012 18:49:34 GMT -5
What place is this?
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Post by labrat1 on Nov 14, 2012 12:57:04 GMT -5
When it comes to medical reasons, you cannot lift such a restriction. I don't think that contacting the IRB will help. You can argue that since you were not told of this before the study began that it is unethical and was entrapment and that you should have been told so that you can choose to opt out of such a study that will disqualify you from a majority of studies afterward.
Do you know who made the restriction? Is it the research facility itself, the study doctor or the sponsor?
It seems that you can only make a big issue of the fact that you were under-informed about the disadvantages of the study.
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Post by vark on Nov 22, 2012 19:03:56 GMT -5
just cross the clinic off your list of clinics. it happens. we can't all go to every clinic.
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