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Local Anesthetic
Buffered 2% lidocaine with 1:100,000 epinephrine for Irreversible Pulpitis
Phase 4
Recruiting
Research Sponsored by Indiana University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 20 minutes post-drug administration
Awards & highlights
Study Summary
The purpose of this study is to determine whether one type of anesthetic (numbing medicine) will work better at numbing the nerve in a tooth than using a different type of anesthetic. A second purpose is to see if the time needed to numb the nerve in a tooth is different between the two anesthetics.
Eligible Conditions
- Irreversible Pulpitis
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 20 minutes post-drug administration
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 20 minutes post-drug administration
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Profoundness of pulpal anesthesia
Secondary outcome measures
Onset of pulpal anesthesia
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Buffered 2% lidocaine with 1:100,000 epinephrineExperimental Treatment2 Interventions
Buffered local anesthetic (addition of sodium bicarbonate to make a 10% buffered solution)
Group II: Unbuffered 2% lidocaine with 1:100,000 epinephrineActive Control1 Intervention
Standard local anesthetic
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Lidocaine
FDA approved
Find a Location
Who is running the clinical trial?
Indiana UniversityLead Sponsor
980 Previous Clinical Trials
982,942 Total Patients Enrolled
Frequently Asked Questions
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