Clinical Trials Directory

Trials / Completed

CompletedNCT03341260

Effect of Preoperative Diclofenac Potassium on Postoperative Endodontic Pain

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

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
70 (actual)
Sponsor
Cairo University · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGDiclofenac Potassium 50mg Tab.A 50 mg tablet of the medication to be taken one hour before initiation of endodontic treatment.
DRUGPlaceboA placebo will be taken one hour before initiation of endodontic treatment.

Timeline

Start date
2016-12-01
Primary completion
2018-02-01
Completion
2018-04-01
First posted
2017-11-14
Last updated
2018-04-09

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03341260. Inclusion in this directory is not an endorsement.