None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients older than 18 years and younger than 60 years of either gender. Mandibular molar teeth diagnosed with symptomatic irreversible pulpitis with apical periodontitis. Patient not taken any medication like analgesic, antibiotic since past 3 days. Cooperative healthy patients who are willing to participate in the study and sign the consent form.
Exclusion criteria
Exclusion criteria: Patients younger than 18 or older than 60 years. Subjects taking any medication such as antibiotics, analgesics, narcotics, sedatives, or antidepressants. History of significant medical problem (ASA III or greater). Tooth that not indicated for further restoration. Subjects unable to give informed consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate and compare the effect of propolis and its combination with calcium hydroxide as an intracanal medicament on postoperative pain in permanent mandibular molars with symptomatic irreversible pulpitis and apical periodontitis.Timepoint: To evaluate and compare the effect of propolis and its combination with calcium hydroxide as an intracanal medicament on postoperative pain in permanent mandibular molars with symptomatic irreversible pulpitis and apical periodontitis at 12,24 and 48 hrs | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NIL | — |
Countries
India
Contacts
Bharati vidyapeeth dental college and hospital, Navi mumbai