Wisdom Tooth Study
Research Question:
Is a combination of non-opioid pain medications just as (or more) effective than opioid-containing
pain medications?
Basic Study Information
Purpose:
If you take part in the research, you will be asked to complete several questionnaires,
to take a pain medication that's provided, and you will be asked to wear an activity
monitor for 72 hours. It will take about 15 minutes during your surgery visit and
post-operative visit to complete questionnaires. During the post-operative period
you will receive electronic messages (via text or email) in the morning and evening.
The messages will ask you to complete an eDiary on your smartphone to record pain
levels, which will take about 2-3 minutes for each entry. Participants must be age
18+, have at least one wisdom tooth impacted in the lower jaw, and be in generally
good health and able to take ibuprofen (Advil, Motrin), acetaminophen (Tylenol), and
hydrocodone.
Location: Eastman Institute for Oral Health
Study Reference #: 00005429
Lead Researcher (Principal Investigator)
Lead Researcher:
Hans Malmstrom
Study Contact Information
Study Coordinator: Stacie Ellis
Phone: (585) 273-4489
Email: stacie_ellis@urmc.rochester.edu
Additional Study Details
Number of Visits:
2 to 5
Parking:
Reimbursed
Reimbursement:
Yes
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