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临床试验/NCT07239154
NCT07239154尚未招募不适用

Clinical and Radiographic Assessment of Injectable Composite Versus Packable Composite in the Restoration of Cavitated Primary Molars a Randomized Clinical Trial

Eslam samy abdel monaem kalboush1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2026年5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
尚未招募
发起方
入组人数
32
试验地点
1
主要终点
Clinical Assessment of Injectable Composite Versus Packable Composite in The Restoration of Cavitated Primary Molars

研究概览

简要总结

This randomized clinical trial aims to compare the clinical and radiographic performance of injectable composite versus packable composite in restoring cavitated primary molars in children aged 4 to 8 years.

Study Purpose

To determine whether injectable composite performs as well as packable composite in Class II restorations in primary molars clinically and radiographically.

详细描述

This randomized clinical trial aims to compare the clinical and radiographic performance of injectable composite versus packable composite in restoring cavitated primary molars in children aged 4-8 years.

Study Purpose

To determine whether injectable composite performs as well packable composite in Class II restorations in primary molars.

Study Design

Type: Randomized clinical trial

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)

盲法说明

outcome assessors

入排标准

年龄范围
4 Years 至 8 Years(Child)
性别
All
接受健康志愿者
否

入选标准

  • •Patients:
  • •Children aged 4-8 years.
  • •Medically free.
  • •Restorable Class II cavities.
  • •Asymptomatic tooth.
  • •Pre-operative radiographic examination:
  • •Absence of periapical or inter-radicular radiolucency.
  • •Absence of widening of periodontal ligaments space.
  • •Absence of internal or external root resorption.

排除标准

  • •Patients:
  • •Uncooperative children.
  • •Unable to attend follow-up visits.
  • •Parents refuse to sign the informed consent.
  • •Children participating in any other clinical trial involving fluoride therapy or other interventions that could directly influence caries development during the study period.
  • •Teeth which were previously restored.
  • •Mobility.
  • •Pre-operative radiographic examination:
  • •Caries extending deep sub-gingivally.
  • •The tooth is about to exfoliate.

研究组 & 干预措施

injectable composite

Experimental

it is a type of zero flow injectable composite used to restore teeth and molars

干预措施: injectable composite (Other)

Packable composite

Other

composite used to restore molars

干预措施: packable composite (Other)

结局指标

主要结局

Clinical Assessment of Injectable Composite Versus Packable Composite in The Restoration of Cavitated Primary Molars

时间窗: Time: T0 = baseline assessment and procedure will be done. T1 =3 months follow up. T2 = 6 months follow up. T3 = One-year follow-up.

Clinical evaluation will be done according to Fédération Dentaire Internationale FDI criteria Scores: Clinically excellent = 1 Clinically good = 2 Clinically sufficient = 3 Clinically unsatisfactory = 4 Clinically poor = 5

次要结局

  • Radiographic Assessment of Injectable Composite Versus Packable Composite in The Restoration of Cavitated Primary Molars.(t = 0 months t2 = 6 months t3 = 12 months)

研究者

发起方
Eslam samy abdel monaem kalboush
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Eslam samy abdel monaem kalboush

Assistant lecturer in pediatric dentistry department delta university

Cairo University

研究点 (1)

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