Pulpotomy using Biodentine in pulpally involved carious young permanent molars
Not Applicable
- Conditions
- Health Condition 1: Z40-Z53- Encounters for other specific health care
- Registration Number
- CTRI/2020/06/025983
- 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
1.Children of age 6-13 years.
2.Pulpally involved carious young permanent molars.
Exclusion Criteria
1.Children above age 13 years.
2.Radiological signs of internal/external resorption.
3.Any radiographic evidence of periapical pathology.
4.Periradicular abscess.
5.If haemostasis is not achieved within 10 min on application of pressure after removal of coronal pulp while doing full pulpotomy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Haematological assessment and Pulpotomyusing Biodentine in pulpally involved carious young permanent molarsTimepoint: Clinical evaluation at baseline, 7 days, 1 month,3 month,6 months and 9 months. <br/ ><br>Radiographic evaluation at baseline, 3 months,6 months, 9 months
- Secondary Outcome Measures
Name Time Method 1. Assessment of bleeding time at root canal orifices after removal of coronal pulpal in carious young permanent molars. <br/ ><br>2.To analyse differential leucocyte count of pulpal blood collected from root canal orifice after extirpationof coronal pulp in carious young permanent molars. <br/ ><br>3. Clinical and radiographic analysis of success of treatment of pulpotomy in pulpally involved young permanent carious molars by Biodentine over a period of 9 monthsTimepoint: Clinical evaluation at 1 week ,1 month then 3 month, 6 month and 9 month. Radiograph taken pre-treatment and post treatment and after 6 months,9 months).