跳至主要内容
临床试验/NCT03202355
NCT03202355终止不适用

The Effect of OrthoPulse Photobiomodulation on the Rate of Tooth Movement During Alignment With Fixed Appliances

Biolux Research Holdings, Inc.4 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2017年4月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
发起方
入组人数
10
试验地点
4
主要终点
Rate of tooth movement in OrthoPulse treated and non-OrthoPulse treated patients

研究概览

简要总结

The aim of this study is to determine efficacy of OrthoPulse photobiomodulation on the rate of tooth movement during alignment for Subjects receiving fixed appliance orthodontic treatment.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
11 Years 至 60 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Presence of permanent dentition
  • Eligible and scheduled for full-mouth, fixed-appliance orthodontic treatment
  • Moderate to severe crowding (LII ≥ 3 mm), with no labio-lingually displaced teeth
  • Class I or Class II malocclusion by ½ cusp or less
  • Non-extraction in both arches
  • Age 11-60
  • Good oral hygiene
  • Non-smoker; non-use of chewing tobacco

排除标准

  • Subject is currently enrolled in another clinical study
  • Subject decided on Invisalign rather than braces
  • Periodontally involved teeth
  • Use of bisphosphonates (osteoporosis drugs) during the study
  • Subject plans to relocate over the treatment period
  • Spaces between anterior teeth
  • Subject has dental implants or an implanted prosthesis
  • Sponsor employees, the Investigator and staff, as well as their immediate family members

研究组 & 干预措施

Group 1 (Control)

Experimental

Subjects assigned to this group receive fixed appliance orthodontic treatment only

干预措施: Fixed Appliance Orthodontic Treatment (Device)

Group 2 (OP1)

Experimental

Subjects assigned to this group receive fixed appliance orthodontic treatment in conjunction with receiving daily OrthoPulse™ treatments.

干预措施: Fixed Appliance Orthodontic Treatment (Device)

Group 2 (OP1)

Experimental

Subjects assigned to this group receive fixed appliance orthodontic treatment in conjunction with receiving daily OrthoPulse™ treatments.

干预措施: OrthoPulse™ (Device)

结局指标

主要结局

Rate of tooth movement in OrthoPulse treated and non-OrthoPulse treated patients

时间窗: From start of treatment until Little's Irregularity Index (LII) reaches less than approximately 2 mm but greater than 0 mm, no more than 6 months after the start of treatment.

Rate of tooth movement will be evaluated based on the duration of time and amount of tooth movement required to reach Little's Irregularity Index (LII) of less than approximately 2 mm but greater than 0 mm, as determined by the qualified investigator.

次要结局

  • Risk of OrthoPulse PBM to the patient.(Participants will be followed for the duration of their orthodontic treatment, an expected average of 1-2 years, depending on the severity of the case)
  • Effect of OrthoPulse PBM on external apical root resorption (EARR)(6 months after the start of orthodontic treatment)

研究者

发起方
Biolux Research Holdings, Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (4)

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