Health Condition 1: null- Patients diagnosed with symptomatic irreversible pulpitis in relation to first or second premolar tooth of either jaw
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Healthy persons, 18-65 years of age reporting to the Department of Conservative Dentistry and Endodontics, Faculty of Dental Sciences, Bangalore with pain in posterior tooth. 2. First or second premolar tooth of either jaw diagnosed as symptomatic irreversible pulpitis. 3. Teeth that could be treated endodontically in one visit 4. Intraoral periapical radiograph showing intact lamina dura and no periapical radiolucency and absence of anatomical obstacles like calcifications in the canals, and no anticipated procedural difficulties. 4. Patients giving no recent history of any antibiotic or analgesic taken.
Exclusion criteria
Exclusion criteria: 1. Known hypersensitivity to diclofenac. 2. Pregnancy or lactation. 3. Patients with history of asthma or allergy to anti-inflammatory drugs. 4. Patients with active peptic ulceration within the last six months 5. Patients undergoing treatment with other NSAIDs or any other analgesics or corticosteroids during the trial period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the effectiveness of transdermal diclofenac patch for post-endodontic pain management.Timepoint: After two days, the effectiveness of transdermal diclofenac patch will be assessed. | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare the effect of transdermal diclofenac patch against oral diclofenac for post-endodontic pain managementTimepoint: After two days, the effect of transdermal diclofenac patch against oral diclofenac for post-endodontic pain management will be compared. | — |
Countries
India
Contacts
Ramaiah University of Applied Sciences