Evaluation of response to partial pulpotomy performed using different dental materials in human subjects
Phase 2
Completed
- Conditions
- Health Condition 1: K040- Pulpitis
- Registration Number
- CTRI/2020/11/029329
- Lead Sponsor
- ITSCDSR
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 110
Inclusion Criteria
1.Age range of 15-45 years
2.Systemically healthy patient
3.Clinical manifestations of reversible pulpitis.
4.Inadvertent pulp exposure during caries excavation, bleeding controlled under pressure at exposure site and vital pulp.
5.Radiographically, the inclusion criterion will be radiolucency involving enamel, dentin and approaching the pulp.
Exclusion Criteria
1.Patients less than 15 years of age,
2.Non-restorable tooth
3.Pathological mobility
4.Pus discharge through the associated sinus tract
5.Swelling of associated tissues
6.Radiographic external or internal resorption
7.Furcal radiolucency
8.Necrotic pulp on exposure
9.Profuse bleeding where haemostasis would not be achieved even after 6 minutes.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain score using VAS Scale <br/ ><br>Pulp vitality using Electronic Pulp Tester <br/ ><br>Periapical changes using Periapical Index <br/ ><br>Timepoint: Preoperatively <br/ ><br>Postoperatively at 2 weeks, 3 months and 6 months <br/ ><br>
- Secondary Outcome Measures
Name Time Method Periapical Index on RadiographsTimepoint: Recall periods( 2 week, 3 months and 6 months postoperatively)