Clinical Trials Directory

Trials / Unknown

UnknownNCT04593160

Efficacy of Preoperative Diclofenac Potassium- Acetaminophen Combination on Anesthetic Success in Patients With Symptomatic Irreversible Pulpitis: a Randomized Controlled Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
72 (estimated)
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- 1000mg acetaminophen combination compared to diclofenac potassium alone or placebo on local anesthetic success and postoperative pain in patients with symptomatic irreversible pulpitis.

Detailed description

Patients with moderate-to-severe preoperative pain are selected. Patients receive either a single-dose of diclofenac potassium (50mg)- acetaminophen (1000mg) combination, diclofenac potassium (50mg) alone or a placebo tablet as a control. All patients will receive the assigned premedication one hour before single-visit root canal treatment. Anesthetic success of inferior alveolar nerve block will be assessed during access and instrumentation. Postoperative endodontic pain is measured at the following time points: 6,12,24,48,72h and 7 days after treatment.

Conditions

Interventions

TypeNameDescription
DRUGDiclofenac potassium- acetaminophen combinationPreoperative single dose of diclofenac potassium(50mg)- acetaminophen(1000mg) combination
DRUGDiclofenac potassiumPreoperative single dose of diclofenac potassium(50mg)
DRUGPlaceboPreoperative single dose of placebo

Timeline

Start date
2021-01-01
Primary completion
2021-12-01
Completion
2022-03-01
First posted
2020-10-19
Last updated
2020-10-30

Source: ClinicalTrials.gov record NCT04593160. Inclusion in this directory is not an endorsement.