Health Condition 1: K040- Pulpitis
Conditions
Interventions
Intervention1: CLINICAL AND RADIOGRAPHIC EVALUATION OF TRIPHALA IN PRIMARY TOOTH PULPOTOMY. Triphala will be test group: In this study Triphala will be used be as pulpotomy agent for dose of half tabl
Sponsors
Rajive gandhi university of health sciences Bangalore
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients aged 5-8 years of age 2. Teeth with pathologic carious or mechanical exposure of vital pulps and teeth with no clinical symptoms or evidence of pulp degeneration, such as spontaneous or nocturnal pain, pain on percussion, history of swelling, or sinus tracts and teeth with no tenderness to percussion, physiologic or pathologic mobility. 3. Radiographically, the recruited teeth should have a normal radiographic appearance with healthy supporting tissues, no signs of internal resorption, or pathologic external root resorption and no periapical or interâ??radicular pathosis, with at least twoâ??thirds of the root remaining (not more than oneâ??third of the root is physiologically resorbed).
Exclusion criteria
Exclusion criteria: 1. Presence of abscess, fistula 2. Non restorable tooth 3. Non willingness to participate 4. Medically compromised conditions
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Clinical and radiographic out come of triphala as a pulpotomy medicament in primary teeth over formacresol for 1,3,6 months.Timepoint: Clinical and radiographic out come of triphala as a pulpotomy medicament in primary teeth over formacresol will be assessed at baseline, 1, 3 and 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| abscence of mobilty, pain , tenderness, swelling, furcation radiolucency, Normal physiologic primary tooth root resorptionTimepoint: 1,3,6 months follow up with clinical and radiographic evaluation | — |
Countries
India
Contacts
Public ContactDr Prashant Babaji
Sharavathi Dental College and Hospital Shimogga
Outcome results
None listed