Health Condition 1: K029- Dental caries, unspecified
Conditions
Interventions
Intervention1: Acemannan (Group 1),: Acemannan sponge (Group 1) will be then placed over the exposed pulp.
Intervention period is for 6 months.
Intervention2: Naringenin (Group 2): Naringenin sponge (
Sponsors
None listed
Eligibility
Inclusion criteria
Inclusion criteria: 1.The patients with age group 18-45. 2.The patients who will give written consent. 3.Healthy patient with pin-point exposed mature and vital permanent molars, with caries or accident-induced pulp exposure will be included in the study. 4.Patient having vital molars with deep caries approaching the pulp.
Exclusion criteria
Exclusion criteria: 1.The patient who won t give written consent and show no compliance. 2.The patient with history of systemic disease that interferes with pulp healing. 3.The molars which have clinical signs and symptoms of irreversible pulpitis, e.g., spontaneous throbbing pain, tenderness to percussion, abnormal tooth mobility, swelling, or sinus tract. 4.The molars which show sign of pulp necrosis. 5.Radiographic evidence of internal or external resorption, inter-radicular bone loss, or periapical pathology. 6.The tooth which are non-restorable.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| No clinical symptoms of pulpitisTimepoint: Baseline , 1 and then 3 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Signs of regeneration are seen.Timepoint: 6 months. | — |
Countries
India
Contacts
Public ContactDr Promila Verma
King Georges Medical University
Outcome results
None listed