None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Systemically healthy patients, aged between 18-60 years, with mandibular and maxillary molars with symptomatic irreversible pulpitis, radiographically-normal periapical area and no pain on biting or percussion. Patients with preoperative pain VAS score of 5-7 will be included in the trial
Exclusion criteria
Exclusion criteria: Pregnant patients, patients with sensitivity or adverse reactions to any of the medications or materials used in this study, those who had used an analgesic during the preceding 6 hours before the treatment, those with irrestorable teeth or teeth with severe periodontal disease or abscess. Patients with active sites of pathosis in the area of injection will be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The POP will be assessed using 10 cm Visual analong scale (VAS). The patient will be assessed over the phone and monitored.Timepoint: 6 hours, 12 hours, 24 hours, 48 hours, 72 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| escape medicine taken or notTimepoint: at 6,12,24,48,72 hours | — |
Countries
India
Contacts
Meenakshi Academy of Higher Education and Research