None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients those who will be diagnosed with symptomatic irreversible pulpitis and symptomatic apical periodontitis of mandibular molar teeth were included into the study. ASA category I, II Patient age group 20-60
Exclusion criteria
Exclusion criteria: Exclusion criteria included ASA category III and above, patients with any prior medications, those allergic to LA, pregnant, and lactating women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| anesthetic and post operative analgesic efficacy expected with addition of magnesium sulfateTimepoint: anesthetic and post operative analgesic efficacy expected with addition of magnesium sulfate. The onset of anaesthesia will be evaluated by EPT for every 1 min until the corresponding vital tooth stops responding. Lip numbness will be considered to check the aesthetic success within 15 minutes.The duration of anaesthesia will be evaluated every 15 min using EPT till the adjacent normal tooth responded on the working side. | — |
Secondary
| Measure | Time frame |
|---|---|
| post operative analgesic efficacy expected with addition of magnesium sulfateTimepoint: anesthetic efficacy expected with addition of magnesium sulfate. Pain data will be collected after access cavity and insertion of files in the canals. The post-operative analgesia will be examined at intervals of 6, 12, 24, and 48 h. | — |
Countries
India
Contacts
Chettinad Dental College and Research Institute