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临床试验/NCT04419805
NCT04419805进行中(未招募)不适用

Single Palatal Temporary Anchorage Device for Anterior Open Bite: a Randomized Clinical Trial

University of Dundee2 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2021年4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
进行中(未招募)
入组人数
32
试验地点
2
主要终点
Molar intrusion

研究概览

简要总结

Participants are orthodontic patients with anterior open bite (AOB) malocclusion. These patients will be treated by molar intrusion achieved using one of two interventions, either orthodontic fixed appliances incorporating a single palatal Temporary Anchorage Device (TAD) or orthodontic fixed appliances incorporating two buccal TADs

详细描述

Participants will be recruited from those attending Dundee Dental Hospital Orthodontic Department and those currently awaiting treatment. Those that meet the inclusion and exclusion criteria will be invited to participate. After obtaining consent they will be allocated to receive one of the two interventions. The two interventions represent the currently available options for treatment of mild - moderate (1-6mm) anterior open bite in the Orthodontic Department and as such patients will be receiving routine treatment regardless of the arm they are randomised to. In order to assess the more effective intervention additional records will be taken during the treatment involving additional cephalometric radiographs, additional intra-oral scans or dental impressions (See later for details). Primary outcome is at the end of intrusion with TADs after 9-12 months, but participants will be followed until completion of treatment for the secondary outcome of stability of intrusion and overbite correction

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
Single (Outcomes Assessor)

盲法说明

Outcome assessor will be blind to allocation

入排标准

年龄范围
12 Years 至 40 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with AOB of 1-6mm
  • Aged between (12 and 40 years).
  • Able to consent.
  • Patient due to undergo orthodontic treatment with fixed orthodontic braces.

排除标准

  • Patient has previously had upper first permanent molar extraction.
  • Patient with congenital cleft of lip and/or palate or any other craniofacial anomalies.
  • Patient with bone disease or taking medications that affect the bone quality or nature.
  • Patient with an active digit sucking habit.
  • Pregnant or breastfeeding women

研究组 & 干预措施

Single Palatal TAD

Experimental

Single Palatal TAD for orthodontic molar intrusion

干预措施: Single Palatal TAD (Device)

Two buccal TADs

Experimental

Two buccal TADs for orthodontic molar intrusion

干预措施: Two buccal TADs (Device)

结局指标

主要结局

Molar intrusion

时间窗: 9-12 months after treatment commences

Amount of upper molar intrusion measured in mms on cephalometric radiograph

次要结局

  • Overbite (vertical overlap of anterior teeth)(9-12 months after treatment commences)
  • Patient Experience(9-12 months after treatment commences)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Peter Mossey

Professor

University of Dundee

研究点 (2)

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