Health Condition 1: null- The subjects having pain in a mandibular molar shall be recruited. They should be in a good health, and none will be taking any medication that would alter pain perception
Conditions
Interventions
Intervention1: Towards side of injection: After the injection, the patients will be divided into two groups on the basis of the position of the head. In the first group, the patients will be asked to
Sponsors
Faculty of Dentistry Jamia Millia Islamia
Eligibility
Inclusion criteria
Inclusion criteria: The inclusion criteria will be: 1.carious exposed symptomatic mandibular molars with signs and symptoms consistent with irreversible pulpitis, 2.a sharp and lingering pain on thermal stimulus and an electric pulp tester, 3.hemorrhaging on access opening.
Exclusion criteria
Exclusion criteria: Exclusion criteria include: 1. known allergy or contraindications to any content of local anesthetic solution, 2.patients who are pregnant or breastfeeding, a history of known or suspected drug abuse, 3. patients taking any drugs that could have affected pain perception. 4.Patients having active pain in more than 1 tooth will be excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Success will be defined as no pain or weak/mild pain during endodontic access preparation and instrumentation Timepoint: The primary outcome will be assessed at the root canal access preparation stage. | — |
Secondary
| Measure | Time frame |
|---|---|
| Injection painTimepoint: The injection pain will be evaluated just after administering the local anesthetic injection. | — |
Countries
India
Contacts
Public ContactDr Vivek Aggarwal
Jamia Millia Islamia
Outcome results
None listed