Using a Narcotic to Enhance the Numbing Effect of the Local Anesthetic Lidocaine on Inflamed Molar Teeth
Launched by NATIONAL INSTITUTE OF DENTAL AND CRANIOFACIAL RESEARCH (NIDCR) · Jan 18, 2000
Trial Information
Current as of March 21, 2025
Completed
Keywords
ClinConnect Summary
The clinical efficacy of local anesthetics is reduced in the presence of inflammation, sometimes limiting the ability to perform necessary therapeutic procedures. Recent studies suggest, however, that opiate receptors are expressed in the dental pulp and oral mucosal tissues and increase in number under conditions of inflammation. The proposed clinical study will assess the therapeutic effectiveness of the opioid, fentanyl, to enhance the profoundness of the local anesthetic lidocaine with 1:100,000 epinephrine when used on inflamed mandibular molar teeth. Delivering lidocaine 2% with 1:100...
Gender
ALL
Eligibility criteria
- • Men and women whose mandibular molars are either: intact, caries-free, and have no signs or symptoms of pulpal disease or carious, symptomatic (to hot/cold and percussion), but have no evidence of pulpal necrosis or infection. At least one intact caries-free contralateral mandibular molar must be present.
- • Individuals should be healthy and over the age of 16.
- • No history of stomach ulcers, asthma, lung problems, or allergy to lidocaine, fentanyl or any of the standard or test medications.
- • No body weight which is 30% greater or less than standard height-weight tables.
- • No pregnant or lactating females. Also, no females who are sexually active and will not submit to a pregnancy test.
- • No history of taking any analgesics or antihistamines for 24 hr period prior to study.
- • No patients taking steroids or other anti-inflammatory drugs.
- • Willing to accept root canal treatment without parenteral sedation.
- • Willing to participate in data collection procedures.
- • No clinically significant medical history or signs of debilitation including patients with heart, respiratory, renal, or liver dysfunction.
- • No history of personality disorder, alcohol abuse or drug abuse.
- • No chronic use of drugs which would confound assessment including barbituates, anticonvulsants, tranquilizers, antiarrythmics, beta blockers, and antidepressants.
- • No patients whose mandibular molars are heavily restored (i.e., crowns, large fillings).
- • No hypersensitivity to drugs used (epinephrine, lidocaine, fentanyl).
About National Institute Of Dental And Craniofacial Research (Nidcr)
The National Institute of Dental and Craniofacial Research (NIDCR) is a pivotal component of the National Institutes of Health (NIH) dedicated to advancing the understanding, prevention, and treatment of dental and craniofacial disorders. Through innovative research and clinical trials, NIDCR aims to enhance oral health and improve the quality of life for individuals affected by these conditions. The institute fosters collaboration among scientists, clinicians, and public health professionals to translate research findings into practical applications, ensuring that the latest advancements benefit patients and communities. With a commitment to excellence in research and education, NIDCR plays a critical role in shaping the future of oral health care.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Bethesda, Maryland, United States
People applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Discussion 0
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