Is a
Clinical Study attributes
NCT Number
Health Conditions in Trial
0
Trial Recruitment Size
110
Trial Sponsor
Clinical Trial Start Date
2008
0Primary Completion Date
2009
0Study Completion Date
2010
0Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Other0
Intervention Type
Drug0
Intervention Name
Bupivacaine0
Lidocaine0
Interventional Trial Phase
Phase 40
Official Name
Comparison of Bupivacaine vs Lidocaine on Inflammatory Regulation Following Endodontic Surgery: A Double-Blind, Randomized, Controlled Clinical Trial0
Last Updated
May 31, 2018
0Allocation Type
Randomized0
Intervention Model
Parallel Assignment0
Masking Type
Triple0
Masked Party
Investigator0
Participant0
Outcomes Assessor0
Study summary
This study is testing a local anesthetic (numbing medicine) to suppress pain. Bupivacaine and lidocaine are FDA approved local anesthetics that may decrease pain following surgery. Patients will receive either 2% lidocaine, 0.5% bupivacaine, or placebo with epinephrine 1:200,000 as a numbing medicine at the end of root canal surgery. Small pieces of gum will be taken before and after surgery and 2 days later to analyze chemicals that may be related to pain sensation.
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Further Resources
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