Status:
COMPLETED
Effect of Post-Operative Anesthetics on Post-Operative Pain in Patients Receiving Endodontic Treatment
Lead Sponsor:
University of Washington
Conditions:
Endodontic Disease
Post Operative Pain
Eligibility:
All Genders
18+ years
Phase:
PHASE4
Brief Summary
This study will assess the efficacy of two local anesthetics (2% lidocaine 1:100,000 epinephrine and 0.5% bupivicaine 1:200,000 epinephrine) in reducing post-operative pain in patients receiving endod...
Detailed Description
The goal of this study is to assess the efficacy of 2% lidocaine 1:100,000 epinephrine and 0.5% bupivicaine 1:200,000 epinephrine in reducing post-operative pain in patients with symptomatic irreversi...
Eligibility Criteria
Inclusion
- Diagnosis of symptomatic irreversible pulpitis on mandibular, posterior tooth
- ASA I or II
- \>18 years old
Exclusion
- Maxillary or mandibular anterior tooth
- Diagnosis of pulp necrosis or reversible pulpitis
- Tooth deemed non-restorable
- \<18 years old
- ASA III, IV, or V
- Patients who are contraindicated to take ibuprofen
- Patients with allergies to any medications being assessed in this study
Key Trial Info
Start Date :
September 29 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 1 2024
Estimated Enrollment :
35 Patients enrolled
Trial Details
Trial ID
NCT05338671
Start Date
September 29 2021
End Date
June 1 2024
Last Update
May 29 2025
Active Locations (1)
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1
University of Washington- School of Dentistry
Seattle, Washington, United States, 98112