| Participants' health, rights and privacy are protected
from study recruitment to result reporting.
Health: The Dental Clinical Research Center has a dedicated
clinical coordinator who provides clinical trial management services for each
phase in a protocol. She is also available to answer your questions
throughout your involvement in the study.
Rights: All human subjects
research carried out at The University of Iowa or under its auspices must be
reviewed by the Institutional Review Board (IRB). Projects that have industry-
sponsored external support must also be reviewed and approved by the Clinical Trials Office and the Human Subjects Office.
Privacy: A participant's privacy is honored throughout the entire
study and beyond. All participants are assigned an unidentifiable alias
number for labeling research data. All staff are trained to uphold
confidentiality when performing research studies. Research presentations and
publications are done without participant names or initials. If
photographs are used, it is only with the permission of the participant.
For more information on
becoming a research participant, please email the
Office of Clinical Research or call us at 319-335-6763.
Follow this link to
Current Clinical Studies being
performed at The Office of Clinical Research.
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