Health Condition 1: K040- Pulpitis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients giving Informed consent for the study Healthy Patients Pre operative moderate to severe pain VAS scale greater than 54 mm Mature Mandibular first or second molars diagnosed with symptomatic irreversible pulpitis No peri apical radiolucency No prior history of root canal treatment
Exclusion criteria
Exclusion criteria: Patients not giving Informed consent for the study Patients whose age is less than 18 years and more than 50 years Patients allergic to local anesthesia or any other component of LA solution to be used in the study Patient having history of medicine intake including corticosteroids opioids NSAIDs tricyclic antidepressants or beta blockers in the past 12 hour Previously initiated or Endodontically treated teeth Drug abusers and alcoholics Pregnant patients Patients with neuropathic disorders chronic pain syndromes genetic and metabolic disorders inflammatory and autoimmune disorders
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Anesthetic success rate No to mild pain indicated by 0 to 54 mm will be considered as successful anesthesia and moderate to severe pain 55 to 170 mm will be denoted as failureTimepoint: using VAS scale at baseline(immediate) | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain on injection will be evaluated by the consultant endodontist immediately after the injection using HP VASTimepoint: using VAS scale at baseline(immediate) | — |
Countries
India
Contacts
JCD dental college sirsa