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In clinical trials of new medicines, half of the subjects

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In clinical trials of new medicines, half of the subjects [#permalink]

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New post 31 Dec 2003, 14:40
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18. In clinical trials of new medicines, half of the subjects receive the drug being tested and half receive a physiologically inert substance ?a placebo. Trials are designed with the intention that neither subjects nor experimenters will find out which subjects are actually being given the drug being tested. However, this intention is frequently frustrated because ____.

Which one of the following, if true, most appropriately completes the explanation?

(A) often the subjects who receive the drug being tested develop symptoms that the experimenters recognize as side effects of the physiologically active drug

(B) subjects who believe they are receiving the drug being tested often display improvements in their conditions regardless of whether what is administered to them is physiologically active or not

(C) in general, when the trial is intended to establish the experimental drug's safety rather than its effectiveness, all of the subjects are healthy

(D) when a trial runs a long time, few of the experimenters will work on it from inception to conclusion

(E) the people who are subjects for clinical trials must, by law, be volunteers and must be informed of the possibility that they will receive a placebo
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New post 31 Dec 2003, 16:57
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Trials are designed with the intention that neither subjects nor experimenters will find out which subjects are actually being given the drug being tested.

As per the expectation either the subjects or the experimenters should know who has been given the drug. But the experimenters come to know because of the side effects.
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In clinical trials of new medicines, half of the subjects receive the [#permalink]

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In clinical trials of new medicines, half of the subjects receive the drug being tested and half receive a physiologically inert substance—a placebo. Trials are designed with the intention that neither subjects nor experimenters will find out which subjects are actually being given the drug being tested. However, this intention is frequently frustrated because______
Which one of the following, if true, most appropriately completes the explanation?
(A) often the subjects who receive the drug being tested develop symptoms that the experimenters recognize as side effects of the physiologically active drug
(B) subjects who believe they are receiving the drug being tested often display improvements in their conditions regardless of whether what is administered to them is physiologically active or not
(C) in general, when the trial is intended to establish the experimental drug’s safety rather than its effectiveness, all of the subjects are healthy
(D) when a trial runs a long time, few of the experimenters will work on it from inception to conclusion
(E) the people who are subjects for clinical trials must, by law, be volunteers and must be informed of the possibility that they will receive a placebo
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Re: In clinical trials of new medicines, half of the subjects receive the [#permalink]

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In clinical trials of new medicines, half of the subjects receive the drug being tested and half receive a physiologically inert substance—a placebo. Trials are designed with the intention that neither subjects nor experimenters will find out which subjects are actually being given the drug being tested. However, this intention is frequently frustrated because______

Which one of the following, if true, most appropriately completes the explanation?

The clinical trials are designed so that no on will know which subject is given the actual drug. To complete the explanation you must find out how this design can be compromised. Essentially, find out what can alert either the subjects or the experimenters who has the real drug.

(A) often the subjects who receive the drug being tested develop symptoms that the experimenters recognize as side effects of the physiologically active drug
Bingo. If the experimenter knows what the symptoms are and the subject is exhibiting the symptoms then the experimenter will know that this subject has the real drug.

(B) subjects who believe they are receiving the drug being tested often display improvements in their conditions regardless of whether what is administered to them is physiologically active or not
This actually will enforce the design. If everyone, including the subjects with the placebo, has the same results then the design holds true. There is no way to figure out who has the real drug or who has the placebo.

(C) in general, when the trial is intended to establish the experimental drug’s safety rather than its effectiveness, all of the subjects are healthy
This is irrelevant. The trial's intent does nothing to compromise the design of the trial.

(D) when a trial runs a long time, few of the experimenters will work on it from inception to conclusion
This does not compromise the design of the trial.

(E) the people who are subjects for clinical trials must, by law, be volunteers and must be informed of the possibility that they will receive a placebo
Whether or the subject is a volunteer does not compromise the design of the trial.
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New post 31 Dec 2003, 16:15
I will go with A.
Though B seems to be close
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New post 31 Dec 2003, 16:39
Correct answer is A. I chose B. If you guys have time please justify your answers. Your reasoning ( right or wrong ) will definitely help me and others.
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New post 31 Dec 2003, 17:08
Hats off to you. Unbelievable reasoning. Fantastic explaination indeed.
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Re: In clinical trials of new medicines, half of the subjects receive the [#permalink]

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New post 11 Dec 2014, 05:41
Choice A is correct. The question states " that neither subjects nor experimenters will find out which subjects are actually being given the drug being tested". If " subjects who receive the drug being tested develop symptoms that the experimenters recognize as side effects of the physiologically active drug" then initial condition is violated
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Re: In clinical trials of new medicines, half of the subjects receive the [#permalink]

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New post 11 Dec 2014, 13:21
ajaym28 wrote:
In clinical trials of new medicines, half of the subjects receive the drug being tested and half receive a physiologically inert substance—a placebo. Trials are designed with the intention that neither subjects nor experimenters will find out which subjects are actually being given the drug being tested. However, this intention is frequently frustrated because______
Which one of the following, if true, most appropriately completes the explanation?
(A) often the subjects who receive the drug being tested develop symptoms that the experimenters recognize as side effects of the physiologically active drug
(B) subjects who believe they are receiving the drug being tested often display improvements in their conditions regardless of whether what is administered to them is physiologically active or not
(C) in general, when the trial is intended to establish the experimental drug’s safety rather than its effectiveness, all of the subjects are healthy
(D) when a trial runs a long time, few of the experimenters will work on it from inception to conclusion
(E) the people who are subjects for clinical trials must, by law, be volunteers and must be informed of the possibility that they will receive a placebo



Can you please post OE for this question??
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Re: In clinical trials of new medicines, half of the subjects [#permalink]

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New post 13 Feb 2016, 00:26
Hello from the GMAT Club VerbalBot!

Thanks to another GMAT Club member, I have just discovered this valuable topic, yet it had no discussion for over a year. I am now bumping it up - doing my job. I think you may find it valuable (esp those replies with Kudos).

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Re: In clinical trials of new medicines, half of the subjects   [#permalink] 13 Feb 2016, 00:26
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