Health Condition 1: K040- Pulpitis
Conditions
Interventions
Intervention1: timing of administration: administration of LA at 9:30,12:30,15:30 and 18:30
Control Intervention1: timing of administration: four groups, timing of administration of LA agent at differ
Sponsors
DrGurdeep Singh Gill
Eligibility
Inclusion criteria
Inclusion criteria: patients giving informed consent for the study,All patients were asked to fill a proforma and those patients with similar diurnal variations (Early risers i.e. at or before 6:30 and sleeping time before 21:30) were selected. Patients above 18 years of age, in good health with symptomatic irreversible pulpitis in mandibular first molars, with moderate to high pain intensity ( >54mm, on a 0-170mm Visual Analog Scale (23)) without any radiographic sign of periapical radiolucency (on intraoral periapical radiograph) were selected.
Exclusion criteria
Exclusion criteria: patients allergic to lignocaine or any other constituents used in the trial, not giving informed consent for the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intra-operative pain (as measured on Heft Parker Visual Analog Scale) during access cavity preparation No pain/Mild pain- success Moderate to severe pain- failureTimepoint: Pain will be recorded before starting root canal treatment(time point 1) and during root canal treatment( time point 2) | — |
Secondary
| Measure | Time frame |
|---|---|
| success of IANB block in patients with Symptomatic irreversible pulpitis at9:30am,at 12:30pm, at 15:30pm and at 18:30pmTimepoint: intraoperative | — |
Countries
India
Contacts
Public ContactDr Gurdeep Singh Gill
JCD Dental College
Outcome results
None listed