Health Condition 1: R52- Pain, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.)Patients with symptomatic irreversible pulpitis reported discomfort in single-rooted premolar teeth in either jaw. 2.)An intraoral periapical radiograph of selected teeth should exhibit intact lamina dura and no periapical radiolucency. 3.) Teeth with lack of any anatomical challenges, such as canal calcifications, with no foreseen procedural complications.
Exclusion criteria
Exclusion criteria: 1.) Teeth with associated periodontal conditions. 2.) People who have previously experienced adverse responses to diclofenac and ketoprofen or other nonsteroidal anti-inflammatory drugs (NSAIDs), such as bronchospasm, shock, and urticarial. 3.) Patients who had active duodenal or stomach ulcers before 6 months. 4.) Patients receiving NSAIDs or corticosteroids during the study. 5.) People with a history of illnesses such as bronchial asthma, epilepsy, inflammatory bowel disease, severe liver or renal insufficiency, dengue fever, and mental or psychological issues. 6.) Women who are pregnant and breastfeeding. 7.) Patients with a history of receiving antibiotics during the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| evaluate and compare the efficacy of two modes of delivery of diclofenac and ketoprofen for postendodontic pain control.Timepoint: 24 hr and 48 hr | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NIL | — |
Countries
India
Contacts
Narsinhbhai Patel Dental College and Hospital