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临床试验/NCT07333872
NCT07333872进行中(未招募)不适用

Evaluation of Pulpotomy, Partial Pulpotomy, and Direct Pulp Capping Using Mineral Trioxide Aggregate in Primary Molars. A Randomized Clinical Trial.

Delta University for Science and Technology1 个研究点 分布在 1 个国家目标入组 96 人开始时间: 2025年6月1日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
96
试验地点
1
主要终点
Spontaneous pain

研究概览

简要总结

A comparative evaluation for three vital pulp therapy techniques in primary molars using the same material (MTA)

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
4 Years 至 7 Years(Child)
性别
All
接受健康志愿者

入选标准

  • articipants were cooperative children (4-7 years) with no systemic diseases or relevant allergies. Eligible teeth were restorable primary second molars with deep carious lesions and a diagnosis of reversible pulpitis,

排除标准

  • spontaneous pain, edema, fistula, pathological mobility, or percussion sensitivity.

结局指标

主要结局

Spontaneous pain

时间窗: 12 months

numeric rating scale (presence or abscence of pain) 0 is best result 10 is the worst

Radiolucency of the periapical or furcation area

时间窗: Follow up for 12 months

measuring tool is x-ray

Spontaneous pain

时间窗: 12 months

numeric rating scale (presence or abscence of pain) 0 is best result 10 is the worst

Radiolucency of the periapical or furcation area

时间窗: Follow up for 12 months

measuring tool is x-ray

次要结局

  • Presence or absence of fistula(12 months)
  • Pathological mobility(12 months)
  • Sensitivity on percussion(12 months)
  • Widening of personal ligament space(12 months)
  • Pathological mobility(12 months)
  • Presence or absence of fistula(12 months)
  • Sensitivity on percussion(12 months)
  • Widening of personal ligament space(12 months)
  • Internal or e ternal resorption(12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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