CTRI/2021/06/033971RecruitingNot Applicable
Partial and full pulpotomy outcomes in cariously exposed permanent posterior teeth using a bioceramic material
Gaurav Kulkarni1 site in 1 country153 target enrollmentStarted: July 6, 2021Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Enrollment
- 153
- Locations
- 1
- Primary Endpoint
- Maintenance of normal pulp vitality and normal periapical tissues
Study Overview
Brief Summary
To evaluate the effect on the outcome of cariously exposed permanent posterior teeth treated with partial/complete pulpotomy using a bioceramic material. The novel (but commercially available) bioceramic material will be placed as the medicament over the amputated pulp stumps and a permanent, well-sealing restoration would be placed on top of it. The biological response would be assessed at fixed follow-up intervals where defined clinical and radiographic parameters will be assessed.
Study Design
- Study Type
- Interventional
- Allocation
- Not Applicable
- Masking
- Not Applicable
Eligibility Criteria
- Ages
- 17.00 Year(s) to 65.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Permanent mature posterior teeth with deep to extremely deep caries 2) Teeth that give positive response to pulp vitality testing 3) Teeth in which vitality is confirmed clinically on gaining access 4) Teeth with or without periapical rarefaction 5) Teeth with probing depth and mobility within normal limits 6) Patients that agree to participate in the study.
Exclusion Criteria
- •Teeth with immature apices 2) Teeth where caries does not result in pulp exposure 3) Teeth with extensive caries that are unrestorable 4) teeth with intraoral/extraoral swelling and/or associated sinus tract 5) teeth subjected to abnormal stresses 6) medically compromised patients, pregnant or lactating women.
Outcomes
Primary Outcomes
Maintenance of normal pulp vitality and normal periapical tissues
Time Frame: 3 weeks, 6 months, 12 months, 24 months
Secondary Outcomes
- Formation of dentinal bridge as assessed radiographically(6 months, 12 months, 18 months, and 24 months)
Investigators
Study Sites (1)
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