HRT Study
4 months ago, I volunteered to be in a HRT study, comparing the products Prempro and Femhrt for side affects. There is no placebo, subjects are given two pills to take, but don't know which they are taking. Of course, after the news about the big study (Woman's Health Initiative) on Prempro being stopped, I thought my study would be stopped, too, but it has not.
Instead, we subjects were sent a copy of "new verbiage" and disclosures from the manufacturer updating and correcting the risks of HRT found in the WHI study. We will be asked to sign a release, stating that we are aware of these risks.
I was told that our study was not being cancelled, because it "only studies the drugs for 9 months, and the other study was stopped because of conditions that developed after 5 years." At first blush, this sounded reasonable. My concern is this: the new verbiage is misleading and not accurate according to the information from the Journal of American Medical Assoc., which states that in the study that was stopped, the increase in Coronary Heart Disease (CHD) occured DURING THE FIRST YEAR, not after 5 years! Also women who have only one of the 6 risk factors for CHD should not take HRT. We were NOT screened for coronary heart disease risk at all before this study (I actually have 3 of the risk factors), AND the new disclosure does not say a word about the incident stroke, heart attack, and coronary thrombosis increasing in the first year.
I feel someone is trying to mislead by not informing the participants accurately and by not screening the participants more carefully for CHD risk. I am well-informed, but the other 499 women in this study may not be. Does anyone know to who's attention can I bring these concerns? I tried to talk to the PHD in charge of this study in my area, but my words fell on deaf ears.
I believe this to be a matter of serious concern. If women are willing to be a guinea pig, they should be given ALL the facts, and they should be properly screened, to avoid jeopardizing their health.
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