跳至主要内容
临床试验/NCT07136155
NCT07136155Enrolling By Invitation不适用

Indirect Pulp Capping Versus Hall Crown Technique for the Management of Deep Dentinal Caries of Primary Molars: A Randomized Controlled Trial.

King Abdullah University Hospital1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2024年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
120
试验地点
1
主要终点
Patient pain perception

研究概览

简要总结

This is a randomized clinical trial that aims to compare the clinical and radiographic success of Hall technique (HT) versus Indirect pulp capping (IPC) for the management of deep dentinal caries in primary molars and to compare the child and parent acceptance of HT versus IPC for the management of deep dentinal caries in primary molars.

详细描述

This is a randomized clinical trial that aims to compare the clinical and radiographic success of Hall technique (HT) versus Indirect pulp capping (IPC) for the management of deep dentinal caries in primary molars and to compare the child and parent acceptance of HT versus IPC for the management of deep dentinal caries in primary molars.

Children aged 4-9 years old presenting with occlusal or proximal carious lesions of primary molars radiographically extending into the inner third or quarter of dentin will be invited to participate in this study. Patients will be randomized into two treatment groups using online block randomization technique (block of 6) and sealed envelope techniques. Time taken for clinical procedure will be recorded by a research assistant prospectively from the time the child sits on the dental chair till the end of procedure. Child pain perception will be recorded during intervention by a blinded research assistant using the Sound Eye Motor scale (SEM). Parental preference and child acceptance for each procedure will be recorded immediately after treatment using parent and child questionnaires. Clinical and radiographic success, and patient satisfaction will be evaluated at 6 and 12 months follow up.

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 9 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Fit and healthy.
  • Occlusal or proximal carious lesions on primary molars radiographically extending into the inner third or quarter of dentin.
  • Vital pulp with no signs or symptoms of irreversible pulpitis, necrosis, or an abscess.
  • No tenderness to percussion, or pathological mobility.
  • No radiographic evidence of interradicular/ periapical radiolucency.
  • Radiographic evidence of a radiopaque dentin layer between the radiolucent caries lesion and the dental pulp
  • Tooth is restorable.
  • Patient has good level of cooperation for the intended procedure.
  • Parents consented for their children to be included in the study.

排除标准

  • Medically compromised children.
  • Irreversible pulpitis or pulp necrosis.
  • Soft and/or hard tissue pathology.
  • Furcal/ periapical pathology.
  • Root resorption exceeding one third of the root.
  • Pathological mobility.
  • Patient has poor level of cooperation for the intended procedure

结局指标

主要结局

Patient pain perception

时间窗: Perioperatively

will be evaluated by an observer (research assistant who will be trained, calibrated, and blinded to the treatment used) and recorded using the Sound, Eyes, and motor scale (SEM);Based on the intensity of the child's discomfort, each parameter is scored into one of four categories (comfort (score 0), mild discomfort (score 1), moderately painful (score 2), and painful (score 3)). The total score can range from 0 to 9, with 9 indicating the highest level of discomfort.

Rate of Radiographic Success

时间窗: 6,12 months

Absence of radiographic pathology in the root and the bone in the inter-radicular area.

Child acceptance of treatment

时间窗: immediately following intervention

Self-reported child acceptance using questionnaire

Parent acceptance of treatment

时间窗: immediately following intervention

Parental acceptance using questionnaire

Rate of Clinical Success

时间窗: 3,6,12 months

Absence of clinical symptoms of spontaneous pain, pain on percussion, pathologic mobility or abscess formation.,assessed through taking pain history and clinical examination.

次要结局

  • Time taken for intervention(Perioperative/Periprocedural: from the moment the child sits in the chair until the intervention is completed.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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