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
| Type | Name | Description |
|---|---|---|
| DRUG | Diclofenac potassium- acetaminophen combination | Preoperative single dose of diclofenac potassium(50mg)- acetaminophen(1000mg) combination |
| DRUG | Diclofenac potassium | Preoperative single dose of diclofenac potassium(50mg) |
| DRUG | Placebo | Preoperative 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.