None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Subjects who give verbal assent and whose parents will give the informed consent. Anterior permanent teeth with traumatic or carious lesions with exposure of pulp. Teeth with minimal periapical changes with sufficient bone support. Teeth that can be restored. Subjects who had not taken any antibiotics since 3 months preceding the treatment will be incorporated in the study.
Exclusion criteria
Exclusion criteria: Presence of signs such as prolonged or spontaneous pain, pathological mobility (Miller s Grade II or more), sensitivity to percussion. The medically compromised patients and patients who had taken antibiotics within three months or require antibiotic during treatment. Non restorable tooth / Perforation of pulpal floor. Radiographic signs of internal/external root resorption. Previously endodontically treated teeth. Uncooperative children
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Difference in Microbial Count of E.Faecalis after access opening and after BMPTimepoint: Difference in microbial count of E. faecalis after access opening and after biomechanical preparation (BMP). The first sample will be collected immediately after access opening, and the second sample will be collected on the same day following completion of BMP. | — |
Secondary
| Measure | Time frame |
|---|---|
| Decrease in E. Faecalis CountTimepoint: Decrease in E. faecalis Count After 1-Week Placement of Intracanal Medicaments Bioceramic-Based Intracanal Medicament, Calcium Hydroxide with Iodoform Paste & Probiotic Paste with Saline. Post-BMP, the intracanal medicament will be placed in the root canal & maintained for a period of 7 days. After 7 days, the intracanal medicament will be removed & a microbiological sample will be collected for evaluation. | — |
Countries
India
Contacts
Sudha Rustagi College of Dental Sciences and Research