A study of blood count of primary teeth during pulp therapy.
Not Applicable
- Registration Number
- CTRI/2022/10/046299
- Lead Sponsor
- SGT University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Children in the age group of 3-9 years
Exclusion Criteria
Teeth with necrotic pulp.
Pathologic mobility, redness and swelling of the vestibule, and sensitivity to vestibular palpation
Radicular or succedaneous permanent teeth follicles pathology.
Confounding history of systemic disease, allergic reactions, and special use of local or systemic drugs.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess level of inflammation in relation to treatment planning related to pulpectomy and pulpotomy. <br/ ><br>Timepoint: The aim of present study is to assess co-relation between hematological status i.e, differential leucocytes count with respect to bleeding time, patients reported signs and symptoms in pulpally involved carious primary teeth indicated for pulpotomy or pulpectomy.
- Secondary Outcome Measures
Name Time Method To assess level of inflammation in relation to treatment planning related to pulpectomy and pulpotomy.Timepoint: The aim of present study is to assess co-relation between hematological status i.e, differential leucocytes count with respect to bleeding time, patients reported signs and symptoms in pulpally involved carious primary teeth indicated for pulpotomy or pulpectomy.