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Sponsored by: |
Albany Medical College |
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Information provided by: | Albany Medical College |
ClinicalTrials.gov Identifier: | NCT00574015 |
This study will compare the degree of pain control provided by two techniques for persons with toothache in an emergency department. The two techniques include;
Condition | Intervention | Phase |
---|---|---|
Toothache |
Drug: hydrocodone/acetaminophen Drug: bupivacaine (supraperiosteal nerve block) |
Phase IV |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study |
Official Title: | The Comparison of Supraperiosteal Nerve Block With Opiate Analgesia in Alleviating the Pain of Toothache |
Estimated Enrollment: | 60 |
Study Start Date: | December 2007 |
Estimated Study Completion Date: | December 2008 |
Arms | Assigned Interventions |
---|---|
oral: Active Comparator
administration of oral analgesia
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Drug: hydrocodone/acetaminophen
oral hydrocodone 10 mg/acetaminophen 650 mg
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Dental Block: Experimental
Administration of supraperiosteal nerve block to effected tooth
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Drug: bupivacaine (supraperiosteal nerve block)
Administration of Bupivacaine 0.5% 2 ml adjacent to tooth root
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Background: Toothache is a common complaint among patients presenting to the emergency department. There are two commonly employed methods of alleviating this severe form of pain. Oral opioid analgesia is the most commonly utilized strategy for treating this pain. However, many emergency physicians and dentists employ a local anesthetic technique known as supraperiosteal nerve block. This study will compare the relative efficacy of these techniques.
Patients meeting enrollment criteria will be randomized to either receive a supraperiosteal nerve block or oral hydrocodone 10 mg/acetaminophen 650 mg. They will otherwise be managed identically. Reduction of pain scores between entry and 30 minutes post intervention will be compared as well as numeric pain scores obtained by phone contact 24 hours later. Secondary outcomes will include the proportion of individuals from each group filling prescriptions for pain medication and the number of pain pills taken.
Ages Eligible for Study: | 18 Years to 65 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Wayne R Triner, DO, MPH | 518-262-3773 | trinerw@mail.amc.edu |
United States, New York | |
Albany Medical Center Hospital | |
Albany, New York, United States, 12208 |
Principal Investigator: | Wayne R Triner, DO, MPH | Albany Medical College |
Responsible Party: | Emergency Medicine, Albany Medical College ( Wayne Triner, DO, MPH ) |
Study ID Numbers: | 2200, 2200 |
Study First Received: | December 13, 2007 |
Last Updated: | December 13, 2007 |
ClinicalTrials.gov Identifier: | NCT00574015 |
Health Authority: | United States: Institutional Review Board |
toothache regional anesthesia emergency department |
Tooth Diseases Facial Pain Facies Toothache Pain Naphazoline Oxymetazoline Signs and Symptoms |
Guaifenesin Phenylephrine Hydrocodone Emergencies Bupivacaine Phenylpropanolamine Stomatognathic Diseases Acetaminophen |
Respiratory System Agents Physiological Effects of Drugs Anesthetics Central Nervous System Depressants Narcotics Pharmacologic Actions Anesthetics, Local Analgesics, Non-Narcotic |
Sensory System Agents Therapeutic Uses Analgesics Peripheral Nervous System Agents Antitussive Agents Central Nervous System Agents Analgesics, Opioid |