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临床试验/ACTRN12612001237875
ACTRN12612001237875尚未招募未知

ndertake a clinical trial that would demonstrate that the implementation of a Minimal Intervention Dentistry approach to a group of community dental patients (adolescents aged 11-14 years) who are at high risk to dental caries is likely to be 'cost-effective' compared to 'current practice' in achieving positive oral health outcomes for this population group.

Dental Health Services Victoria0 个研究点目标入组 504 人开始时间: 2012年11月22日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
入组人数
504

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Prevention
盲法
Blinded (masking used)

入排标准

年龄范围
11 Years 至 14 Years(—)
性别
All

入选标准

  • Adolescent patients aged 11 -14 years who:
  • 1.are holders of or dependents of a Health Care Card or Concession Card AND
  • 2.attend their 12 months high-risk recall visit and completed their general course of care AND
  • 3.are assessed as having developed more than one carious lesion in the last 12 months (including white spot lesions) AND
  • 4.have had all occlusal fissures of premolars,molars and partially erupting molars sealed

排除标准

  • Exclusion criteria for this study include:
  • methamphetamine users and drug addicted patients
  • patients with diagnosed medical conditions that may, in the opinion of the investigators, compromise the study outcome
  • e.g. requiring anticoagulant therapy, chemotherapy or radiotherapy, congenital heart disease.
  • patients with a diagnosed intellectual or mental health condition which may impair the patient’s comprehension of the MID protocol instructions and their capacity to meet Study requirements
  • patients with diagnosed physical disabilities that inhibit the patient from performing the oral health care instructions as part of the MID protocol
  • patients with more than four deciduous molars remaining
  • adolescents undergoing fixed or removable orthodontic treatment
  • An allergy to milk protein (not lactose intolerance). (Applies to intervention group only)
  • An allergy to the preservative, Sodium Benzoate (Applies to intervention group only)
  • History of severe asthma, requiring hospitalisation (Applies to intervention group only)

研究者

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