None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patient presenting with chronic apical periodontitis in the Maxillary Anterior teeth with periapical lesions as seen on the radiograph Patient provides informed consent
Exclusion criteria
Exclusion criteria: Unwilling patients Patients with obstructed canals Smokers and alcoholics Pregnant and lactating women Periodontally compromised teeth Patients with bleeding disorders Patients who have an allergy to Simvastatin Patients on oral Simvastatin
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction in size of periapical lesion in maxillary anterior teeth after using simvastatin, calcium hydroxide as intra canal medicamentTimepoint: 1 month 3 months 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Effectiveness of simvastatin hydrogel as an intra canal medicamentTimepoint: 1 month 3 months 6 months | — |
Countries
India
Contacts
Army College of Dental Sciences