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Effect of Preoperative Diclofenac Potassium on Postoperative Endodontic Pain

Pulpitis - Irreversible Clinical Trial

Official title:
Effect of Preoperative, Single-dose Diclofenac Potassium on Postoperative Endodontic Pain in Patients With Symptomatic Irreversible Pulpitis: A Double Blind Randomized Controlled Trial

Clinical Trial Summary

The purpose of this study is to assess the effect of preoperative a single-dose of 50 mg diclofenac potassium on postoperative endodontic pain in mandibular molars with symptomatic irreversible pulpitis.

Clinical Trial Description

Patients with moderate-to-severe preoperative pain are selected. Patients receive either a single-dose of 50 mg diclofenac potassium (group A) or a placebo tablet as a control (group B). All patients receive the assigned premedication one hour before single-visit root canal treatment. Postoperative endodontic pain is measured at the following time points: 6 , 12,24,48 h after treatment. The incidence of analgesic intake is also recorded. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03341260
Study type Interventional
Source Cairo University
Contact
Status Completed
Phase Phase 2/Phase 3
Start date December 2016
Completion date April 2018
View Details
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