Towards predicting the analgesic response to ibuprofen following third-molar extraction

Recruiting
18 years - 64 years
All
Phase
N/A
80 participants needed
1 Location
Brief description of study
NSAIDs like ibuprofen are pain relievers that are commonly used to reduce pain after dental procedures.
Patients
who have their impacted third molar teeth taken out usually experience pain one
to three hours after surgery and require pain relievers for at least 2 days. Most
people (about 70-90%) experience good to excellent relief of their pain when
they take ibuprofen. However, some patients experience only limited pain
relief with ibuprofen, and a few experience no pain relief at all. These
patients need a different type of pain reliever added to their regimen. The purpose
of this study is to see if there are substances in your blood and urine which we
will take both before and after your wisdom teeth surgery that can tell us how
you personally will respond to
ibuprofen in comparison to placebo (an inactive sugar pill). We will also study
how well ibuprofen combined with acetaminophen works for up to 7
days after surgery.
Detailed description of study
There are 4 study visits:
1) Screening - patients read and sign
informed consent, urine and blood sample are taken, fill out
questionnaire about mood and pain expectations.
2) Surgery - Swab of mouth to
collect bacteria, urine and blood sample taken prior to surgery. Have
surgery performed standard of care, receive study medication (ibuprofen
400 mg or placebo), multiple urine and blood samples (through indwelling
catheter) taken, pain assessments taken, discharged with ibuprofen
400mg/acetaminophen500mg taken q4h and oxycodone 5mg if needed
3)
24 Hour Follow-up - Return visit with a single blood and urine sample
4) Day 7 Follow-up - Return visit with a single blood and urine sample
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Impacted Third Molar Tooth | Pain,Acute
-
Age: 18 years - 64 years
-
Gender: All
Study participants must be in reasonably good health and require
the removal of at least one mandibular partial or full bony impacted third
molar (wisdom tooth).
Updated on
19 Feb 2024.
Study ID: 832417