Reversible Pulpitis Clinical Trial
Official title:
Effect of Different Liners on Pulpal Outcome and Survival of Composite Restorations After Partial Caries Removal: A Randomized Controlled Study.
Verified date | January 2018 |
Source | Postgraduate Institute of Dental Sciences Rohtak |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Aim of the study was to determine the effectiveness of cavity liners regarding survival of
restoration beneath composite restoration after partial caries removal in permanent teeth
with deep caries and to evaluate and compare the pulp vitality outcome both clinically and
radiologically with and without liners.
Study was conducted in Post Graduate Institute of Dental Sciences, Rohtak in department of
Conservative Dentistry & Endodontics. Mature permanent mandibular molars with deep dentinal
caries and without any signs of irreversible pulpitis were included in the study. After
partial excavation of caries, patients were randomly allocated into three groups- RMGIC, CH
and DIRECT COMPOSITE group and were restored according to standard protocol.
Status | Completed |
Enrollment | 198 |
Est. completion date | January 25, 2018 |
Est. primary completion date | January 25, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 14 Years to 54 Years |
Eligibility |
Inclusion Criteria: - Patient willing to participate in the study. - Mature permanent mandibular molars with deep dentinal caries involving more than half or two thirds of dentin. Exclusion Criteria: - Primary teeth. - Teeth with irreversible pulpitis (spontaneous pain) or pulp necrosis, chronic periodontitis, cracked tooth, internal or external resorption, calcified canals, associated with sinus tract, and furcation or apical radiolucency. - Immuno-compromised, diabetic, pregnant and hypertensive patients. - Positive history of antibiotic and analgesic use. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Postgraduate Institute of Dental Sciences Rohtak |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Evaluate and compare the clinical and radiographic success with different liners after partial caries excavation | CRITERIA FOR SUCCESSFUL OUTCOME The Presence of positive response to vitality tests, absence of tenderness or spontaneous pain will be considered as clinical signs of success while absence of any radiolucency in periapical or furcation region or root resorptions as radiographic signs of successful outcome. CRITERIA FOR FAILURE The presence of negative vitality tests, spontaneous pain, fistula, swelling, mobility will be considered as clinical signs of failure while presence of any radiolucency in furcation or periapical region, internal or external root resorption as radiographic signs of failure. Although the procedure of partial caries excavation will be considered fully successful only when it shows successful outcome both from maintaining pulpal vitality as per primary outcome measures and intact restoration as per secondary outcome measures described below. |
The patients were recalled periodically at 1 month, 3months, 6 months and 12 months after the procedure. | |
Secondary | Evaluate and compare the effect of different liners on survival of composite restorations after partial caries excavation. | Treatment outcome will be judged on the basis of clinical findings and photographs recorded at the the baseline and at follow up visits on the basis of FDI criteria as described by Hickel et al. Primary measurement variable will be restoration Retention/Fractures. But the secondary measurable variables will also be evaluated namely Marginal adaptation, Marginal staining, Postoperative sensitivity and Recurrence of caries. Scoring will range from 1( very good), 2(good, after correction very good), 3(sufficient/satisfactory, minor shortcomings), 4 (unsatisfactory, but repairable) to 5 ( poor, replacement necessary). Restorations rated 4 or 5 in one of the criteria will be classified as clinically unacceptable, excluded from further assessment and will be repaired or replaced |
The patients were recalled periodically at 1 month, 3months, 6 months and 12 months after the procedure. |
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