38. know the pros and cons of clinical trials.
my previous post (“the facts and fears of clinical trials”) outlined the basics of market trials but there is still a lot to consider; it’s best not to make a hasty decision either way when deciding whether or not to participate. on one hand, you would be assisting with research, most of which experiences years of delay due to lack of participation in the testing process. on the other hand, there are risks and inconveniences, not to mention eligibility, to consider.
pros: participating in clinical trials will help to advance medical care and possibly help researchers find cures faster. cons: they require a time commitment and also may incur costs not covered by your healthcare plan. some trials require travel or even a hospital stay. pros: you will receive free drugs and frequent, intensive health monitoring. cons: you may not receive the experimental agent or it may not be effective. also, many medications have complex dosage requirements. pros: the satisfaction of helping others. cons: possible adverse side effects, such as life-threatening toxicities developed over time.
ultimately, whatever you decide should be based on facts and supported by research. know your options and your rights. be aware of what a particular study entails before you agree to participate. whether you accept or decline a request to join you will have peace of mind if you feel confident in your decision.
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