CITI ALL MODULES EXAM 200 QUESTIONS WITH
VERIFIED CORRECT AND UPDATED ANSWERS (100%
CORRECT) /A+ GRADE/2023 VERSION
The Belmont Report's principle of
... [Show More] respect for persons incorporates at least two ethical
convictions: first, that individuals should be treated as autonomous agents, and second,
that: - Correct answer-Persons with diminished autonomy are entitled to protection.
Which of the following are the three principles discussed in the Belmont Report? -
Correct answer-Respect for Persons, Beneficence, Justice
Which of the following is an example of how the principle of beneficence can be applied
to a study employing human subjects? - Correct answer-Determining that the study has
a maximization of benefits and a minimization of risks.
An investigational biologic administered to the first two subjects in a Phase II clinical trial
was not appropriately screened for two viral contaminants, HIV and Hepatitis B, due to
human error in the screening process. Follow-up testing indicated that the subjects and
their partners were not infected. The subjects and others were notified of the increased
risk. - Correct answer-This is an unanticipated problem requiring notification to the IRB
and FDA
Housekeeping employees of the medical center were recruited for a federally funded
study of blood pressure, blood count levels, infectious disease history, and job stress.
The interviews and blood tests were conducted in a private location not affiliated with
the study center. Follow-up interviews were conducted in the same location. The study
coordinator stopped at the cafeteria on her way back to the study office after the second
study visit for the last three study subjects and lost the three file folders. Records of one
subject indicated he had a history of a sexually transmitted disease and another had
recently been treated for tuberculosis. The subjects were notified of the loss. Following
this event, the IRB approved a protocol change requiring that all records be transmitted
electronically to the study office using the medical center's secure network. - Correct
answer-This is an unanticipated problem and not an adverse event.
A Data Safety Monitoring Board report for an investigator-initiated investigational drug
study indicates a significantly higher than anticipated rate of an expected adverse event.
This event required revision of the informed consent form to disclose the higher rate. A
change in the eligibility criteria of the protocol to reduce the risk was implemented.
Current subjects would be reconsented. - Correct answer-This is an unanticipated
problem
A subject received the wrong study drug resulting in severe nausea and vomiting, and a
visit to the emergency room for treatment. The subject notified the study coordinator the
day after the emergency room visit. The study coordinator reviewed the subject's study
records and discovered the error. The coordinator notified the subject of the study drug
CITI ALL MODULES EXAM 200 QUESTIONS WITH
VERIFIED CORRECT AND UPDATED ANSWERS (100%
CORRECT) /A+ GRADE/2023 VERSION
error, which caused the nausea and vomiting. The investigator notified the IRB and the
IRB approved a revision of the standard pharmacy procedure for administering
investigational drugs. - Correct answer-This is an unanticipated problem, which resulted
in an adverse event.
A study requires that each subject be given two study drugs. The first study drug is
given on Day 1. A second study drug is given on Day 7 to counteract the toxicity of Drug
1. Subject # 4-706 is given Drug 1 on Day 1. Due to a snowstorm, Subject 4-706 is
delayed for several days before returning to the site for Drug 2. Missing the
administration of Drug 2 on Day 7 placed the subject at risk of significant toxicity. This
event required the subject be notified of the increased risk and required close
monitoring of the subject by phone. - Correct answe [Show Less]