A clinical trial to study the effects of two light cured indirect pulp capping agents
- Conditions
- Dental caries, unspecified,
- Registration Number
- CTRI/2024/01/061916
- Lead Sponsor
- College of dental sciences and research center
- Brief Summary
A Randomized Controlled Clinical Trial to compare two light cured indirect pulp capping agents: an in-vivo study
**Aim:**
This study aims to evaluate the prognostic value of factors with regard to the treatment outcome of indirect pulp capping using Biner LC (METABIOMED Co. LTD) and Hydrocal LC (Medicept Co. Ltd) in permanent posterior teeth having Remaining Dentin Thickness (RDT) of less than or equal to 1**.**5 mm.
**Material and method:**
40 teeth with deep carious lesions and RDT of less than or equal to 1**.**5 mm are selected for indirect pulp capping. Patients are randomly divided into Biner LC and Hydrocal LC groups (n=20 in each group). The patients would be followed up at interval of 1 week, 1 month, 3 months and 6 months with a routine examination on all recall visits. Periapical radiographs would be taken, lack of patient complaints, positive reactions to electric pulp testing, no sensitivity to percussion, and no widening of the periapical ligament indicated success.
**Statistical Analysis:**
The results would be analysed via One way ANOVA test, Chi square test and Paired t- test .
Data would be collected and statistically analyzed.
**Various prognostic factors would be analyzed in this study for the significance of indirect pulp capping agents.**
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 40
Posterior Teeth having occlusal or proximal deep carious lesion, Healthy periodontium.
Teeth with pulp exposure, Sinus opening, Mobility, Cracked tooth.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the pain and tooth sensitivity after treatment long-term outcome of Biner LC over Hydrocal LC as an indirect pulp capping material. The outcome would be assessed at baseline, 1 week,1 month, 3 months and 6 months
- Secondary Outcome Measures
Name Time Method To observe whether any periapical lesion is developing or not via radiographs during follow up periods At 1 week, 3 months & 6 months period during follow up after treatment is provided
Trial Locations
- Locations (1)
College of Dental Sciences and Research Center
🇮🇳Ahmadabad, GUJARAT, India
College of Dental Sciences and Research Center🇮🇳Ahmadabad, GUJARAT, IndiaDr Shilpa ShahPrincipal investigator9376121229drshah16@gmail.com