Originally published January 17 2006
Alliance informs readers of what they should do before agreeing to participate in medical research
by Mike Adams, the Health Ranger, NaturalNews Editor
The Alliance for Human Research Protection provides readers with a checklist and a bevy of information that they should know before giving their informed consent to medical researchers.
The ALLIANCE FOR HUMAN RESEARCH PROTECTION (AHRP) is launching a similar campaign to help ordinary citizens protect themselves from harmful, or unwanted medical research.
AHRP urges anyone considering taking part in a research project to become informed, to speak up, and to ask the questions suggested below.
The doctor conducting the project should provide the answers in writing.
AHRP agrees with the advice JCAHO gives patients: "Don't be afraid to seek a second opinion.
If you are unsure about the nature of your illness and the best treatment, consult with one or two additional specialists.
AHRP urges you to obtain full information about the risks and possible benefits, if any, before signing any consent to research.
Medical researchers do not always inform you (or your family) about the nature of the known and foreseeable risks, discomfort, and possible adverse consequences of medical research.
We therefore suggest that anyone considering taking part in a research project should obtain full information, then seek an independent opinion from a doctor not affiliated with the research team to help you make an informed decision.
Will I be reimbursed for expenses I incur while participating in the study, such as parking fees, meals, pro-rated child expenses, etc?
4. Does this protocol include investigational drugs not approved by the FDA?
If I get a placebo, what is the benefit for me from participating?
7. Is this study designed to benefit me by testing a product or procedure that has a probability of improving my condition?
8. Does the study require that I stop taking all medications (drug "washouts")?
Can I have a family member or trusted friend as an advocate?
Will my record be sent to my doctor to help guide his decisions about my follow-up care?
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