Intranasal Ketorolac for Postsurgical Pain in Dental Implant Patients

Completed · Phase 4

Conditions studied: Acute Pain

In brief

The surgical placement of dental implants is presently a common procedure performed by oral surgeons, periodontists, and general dentists. The surgery can be performed under local anesthesia and involves the incision of soft tissue to expose the underlying bone, preparation of the implant site using a specialized surgical drill, and.screwing the implant into bone using a specialized headpiece. Dental implant patients experience postoperative pain yet there are no studies in the literature which have evaluated the efficacy of analgesics in this patient population. The current pilot study will evaluate the analgesic effects and tolerability of a recently FDA-approved analgesic formulation of intranasal ketorolac (SPRIX®) in 25 patients who have 1 - 3 dental implants surgically placed. Patients will self administer the ketorolac nasal spray (one spray in each nostril, 31.5 mg total dose) when their postoperative pain reaches at least a moderate severity. Pain intensity and pain relief scores will then be recorded every 20 minutes for the first hour, at 1.5 and 2 hours and then hourly through 6 hours on a validated analgesic diary. Side effects will be recorded when and if they occur. Patients will then transition to a multi-dose phase where they will be allowed to dose with ketorolac as indicated in the package insert (up to 4 times per day for 5 days). Patients will record the time of each dose, a daily assessment of overall efficacy and side effects, and the use of any rescue medication (acetaminophen 650 mg) on a take home diary.

Key facts

Study ID

NCT01490931

Run by

Hersh, Elliot V., DMD, MS, PhD

People needed

28

Starts

2011-11-01

Expected to finish

2012-08-01

Last updated by the study team

2014-05-09

Who can join

Age: 18 and older, up to 64. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Key Inclusion Criteria
• Male or female between 18 and 64 years of age.
• Must sign informed consent prior to initiation of any study procedures. The subject must be able to understand and agree to cooperate with study requirements.
• BMI between 19 and 29 kg/m2.
• Must require the surgical placement of 1 - 3 dental implants that are being placed in a one or two stage non-immediately loaded surgical procedure employing 2% lidocaine and/or 4% articaine with epinephrine and/or 3% mepivacaine plain for local anesthesia.
• Females of child-bearing potential must have a negative urine pregnancy test at screening and immediately prior to the initiation of dental implant surgery and must have been using adequate means of birth control (abstinence, oral contraceptive steroids, intrauterine device (IUD), etc.) for at least one month prior to study entry and during the study.
• In the opinion of the investigators the subject can safely tolerate ketorolac and acetaminophen.

You may not qualify if…

• Key Exclusion Criteria
• Require the placement of more than 3 implants or require extensive bone grafting in addition to implant placement.
• Need to administer anxiolytic/sedation drugs during surgery other than nitrous oxide/oxygen.
• Need to administer the long acting local anesthetic bupivacaine with 1:200,000 epinephrine.
• Implant(s) that are going to be immediately loaded on the day of surgery
• Females that are pregnant or breast feeding
• Allergies or hypersensitivity (aspirin sensitive asthma) to ketorolac, aspirin, ibuprofen, other NSAIDs, or acetaminophen.
• History of gastrointestinal ulcers and/or bleeding.
• On warfarin, dicumarol, clopidogrel or any other anticoagulant or antiplatelet therapy other than low dose (81 mg - 325 mg) aspirin.
• Clinically significant kidney or liver disease where the intake of NSAIDs or acetaminophen would put the subject at undo risk.
• Blood pressure greater than 160/95 at the time of screening or immediately before surgery.
• Inflammation of the nasal mucosa or upper respiratory tract infection
• Have ingested any analgesic agent within 48 hours of surgery.

Where it is running

• University of Pennsylvania School of Dental Medicine — Philadelphia, Pennsylvania, United States

Full record on ClinicalTrials.gov

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