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

Phase 4

Completed

• Conditions: Endodontic Disease; Post Operative Pain; Symptomatic Irreversible Pulpitis

• Registration Number: NCT05338671
• Lead Sponsor: University of Washington

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-6-19
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Inclusion Criteria:<br><br> - Diagnosis of symptomatic irreversible pulpitis on mandibular, posterior tooth<br><br> - ASA I or II<br><br> - >18 years old<br><br>Exclusion Criteria:<br><br> - Maxillary or mandibular anterior tooth<br><br> - Diagnosis of pulp necrosis or reversible pulpitis<br><br> - Tooth deemed non-restorable<br><br> - <18 years old<br><br> - ASA III, IV, or V<br><br> - Patients who are contraindicated to take ibuprofen<br><br> - Patients with allergies to any medications being assessed in this study

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Post-operative pain level 6 hours on a visual analog scale;Post-operative pain level 12 hours on a visual analog scale;Post-operative pain level 24 hours on a visual analog scale;Post-operative pain level 48 hours on a visual analog scale;Post-operative pain level 72 hours on a visual analog scale

Secondary Outcome Measures

Name	Time	Method
Over the counter analgesic use