Comparative evaluation of success rate of calcium hydroxide, calcium silicate, and resin modified calcium silicate for indirect pulp capping in permanent molars: a randomised clinical trial.
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 110
- 试验地点
- 1
- 主要终点
- Clinical assessment of pain, swelling, vitality test and pathologic mobility along with radiographic assessment of periradicular architecture and root resorption
研究概览
简要总结
RESEARCH QUESTION
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What is the success outcome of Indirect Pulp Capping with Calcium Hydroxide in permanent molars with extremely deep caries diagnosed with reversible pulpitis.
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What is the success outcome of Indirect Pulp Capping with Calcium Silicate in permanent molars with extremely deep caries diagnosed with reversible pulpitis.
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What is the success outcome of Indirect Pulp Capping with Resin modified Calcium Silicate in permanent molars with extremely deep caries diagnosed with reversible pulpitis.
Aim:
The aim of this randomized clinical trial will be to evaluate and compare the success rate of Calcium Hydroxide, Calcium Silicate, And Resin Modified Calcium Silicate as Indirect pulp capping agents in patients with extremely deep caries in permanent molars diagnosed with reversible pulpitis.
Objectives:
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To evaluate the success of Calcium Hydroxide as an indirect pulp capping material in permanent molars with extremely deep carious lesions diagnosed with reversible pulpitis.
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To evaluate the success of Calcium Silicate as an indirect pulp capping material in permanent molars with extremely deep carious lesions diagnosed with reversible pulpitis.
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To evaluate the success of Resin Modified Calcium Silicate as an indirect pulp capping material in permanent molars with extremely deep carious lesions diagnosed with reversible pulpitis.
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To statistically evaluate and compare success of Calcium Hydroxide, Calcium Silicate, And Resin Modified Calcium Silicate as indirect pulp capping materials in permanent molars with extremely deep carious lesions diagnosed with reversible pulpitis.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 40.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients in the age group of 18-40 years
- •Healthy patients with ASA I and ASA II.
- •Permanent molars with extremely deep caries penetrating the entire thickness of dentin and diagnosed with reversible pulpitis.
- •Teeth that can be easily restored with composite resin.
排除标准
- •Patients with permanent molars diagnosed with irreversible pulpitis or pulp necrosis.
- •Teeth exhibiting tenderness on percussion, sinus tract, mobility, furcation, PDL widening, or periapical radiolucency.
- •Teeth that are not conducive to rubber dam application.
- •Pregnant and lactating mothers.
- •Patients who are hypersensitive to NSAIDS and antibiotics.
结局指标
主要结局
Clinical assessment of pain, swelling, vitality test and pathologic mobility along with radiographic assessment of periradicular architecture and root resorption
时间窗: 3 months, 6 months and 12 months
次要结局
- Pain(24hours, 48 hours and 7 days)
研究者
Dr Jayish Singh
J.N Kapoor DAV(c) Dental college