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Phase 4 N=35 Randomized Single-blind Treatment

Effect of Post-Operative Anesthetics on Post-Operative Pain in Patients Receiving Endodontic Treatment

Endodontic Disease · Post Operative Pain · Symptomatic Irreversible Pulpitis

Enrolled (actual)
35
Serious AEs
0.0%
Results posted
May 2025
Primary outcome: Primary: Post-operative Pain Level 6 Hours on a Visual Analog Scale — 64.2; 43.1 units on a scale

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Local anesthetic (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Washington
Primary completion
Jun 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Post-operative Pain Level 6 Hours on a Visual Analog Scale
64.2; 43.1
PRIMARY
Post-operative Pain Level 12 Hours on a Visual Analog Scale
67.4; 45.1
PRIMARY
Post-operative Pain Level 24 Hours on a Visual Analog Scale
48.9; 36.5
PRIMARY
Post-operative Pain Level 48 Hours on a Visual Analog Scale
45.3; 30.1
PRIMARY
Post-operative Pain Level 72 Hours on a Visual Analog Scale
35.5; 21.9

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 endodontic treatment.

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of symptomatic irreversible pulpitis on mandibular, posterior tooth
  • ASA I or II
  • >18 years old

Exclusion Criteria

  • 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
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05338671). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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