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
| Type | Name | Description |
|---|---|---|
| DRUG | Diclofenac Potassium 50mg Tab. | A 50 mg tablet of the medication to be taken one hour before initiation of endodontic treatment. |
| DRUG | Placebo | A 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.