CTRI/2019/06/019949
Completed
Phase 4
Comparative Evaluation of Post Operative Sensitivity in Non Carious Cervical Lesions restored with Giomer and Nanoceramic composite Resin- An In Vivo Study
Dr Surbhi Gupta0 sites120 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Dr Surbhi Gupta
- Enrollment
- 120
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Patients with at least 24 natural teeth
- •2\.Patients having at least 2 contralateral teeth with non carious cervical lesions indicated for restoration
- •3\.Depth of lesions being \<1 mm and cervico\- occlusal height \<2mm
- •4\.Patients willing to participate in study for 6 months
- •5\.Patients with good oral hygiene
Exclusion Criteria
- •1\.Carious teeth
- •2\.Patients with history of spontaneous pain / sinus tract
- •3\.Patients with class V lesions extending below cemento\-enamel junction
- •4\.Patients having parafunctional habits
- •5\.Patients using any desensitizing toothpaste or mouthwash
- •6\. Patients with active periodontal disease or those who have undergone periodontal surgery during last 6 months
- •7\.Patient allergic to resin based materials
- •8\.Asthmatic patients
- •9\.Patients taking regular NSAIDS, psychotropic drugs or medications for other systemic diseases
- •10\.Pregnant or lactating mothers
Outcomes
Primary Outcomes
Not specified
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