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临床试验/NCT06973057
NCT06973057Enrolling By Invitation不适用

Direct Pulp Capping Versus Pulpotomy Using Neo MTA for Carious Primary Molars: a Split Mouth Randomized Clinical Trial

King Abdullah University Hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
60
试验地点
1
主要终点
Clinical success

研究概览

简要总结

Dental caries is one of the most prevalent chronic diseases worldwide. Interventions for treating deep carious lesions in teeth with no history of pain or teeth with reversible pulpitis are referred to as vital pulp therapy; these include indirect pulp treatment (IPC), direct pulp capping (DPC), and pulpotomy. Pulpotomy is considered invasive when treating exposed primary vital pulps due to caries. Less invasive vital pulp treatment methods such as DPC might, therefore, be preferable, as they reduce chair time, less tooth structure removal and a crown might not always be a necessary permanent restoration. The aim of this clinical study is to evaluate the clinical and radiographic outcomes of DPC when compared to pulpotomy in primary molars with carious pulp exposure.

详细描述

Aim: The aim of this study is to evaluate the clinical and radiographic outcomes of direct pulp capping (DPC) when compared to pulpotomy in primary molars with carious pulp exposure using a calcium silicate-based material: neo mineral trioxide aggregate (Neo MTA).

Methods: The study will be a split mouth randomized clinical trial including children between 4-9 years old. Patients will be allocated into two treatment groups; one group will start with DPC first followed by pulpotomy on the second visit, and vice versa for the second group. The time interval between both visits will be 1-2 weeks. The pulp medicament capping material (neo MTA) will be applied over the exposure site, and then tooth will be restored with glass ionomer cement and then a crown will be placed. Cases will be followed up to 24 months after initial treatment.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
4 Years 至 10 Years(Child)
性别
All
接受健康志愿者
是

入选标准

  • •Healthy patients.
  • •Age 4-10 years.
  • •Primary molar with deep caries present bilaterally.
  • •Teeth should be restorable.
  • •Clinically normal asymptomatic tooth or symptoms of reversible pulpitis (No history of pain or provoked pain subsides upon removal of the stimulus).
  • •Radiographically: caries in the inner half of the dentin approaching the pulp.

排除标准

  • •History of spontaneous pain.
  • •Soft and hard tissue pathology.
  • •Mobility or exfoliating tooth.
  • •No pulp exposure after caries excavation.
  • •Inability to achieve hemostasis after 6 minutes.
  • •Radiographically: Root resorption exceeding 1/3 of the root, apical pathology.

研究组 & 干预措施

Pulpotomy

Active Comparator

The entire coronal pulp will be amputated.

干预措施: Pulpotomy (Procedure)

Direct pulp capping

Active Comparator

The exposure site will be left intact, no amputation of pulp tissue.

干预措施: Direct pulp capping (DPC) (Procedure)

结局指标

主要结局

Clinical success

时间窗: 24 months

No post-treatment signs or symptoms such as sensitivity, pain, mobility or swelling should be evident.

Radiographic success

时间窗: 24 months

No radiographic evidence of pathologic external or internal root resorption, periapical or furcation radiolucency.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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