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临床试验/NCT03450551
NCT03450551Unknown不适用

Comparison of Clinical Efficacy of Three Class II Correctors in Orthodontics, Prospective Expertise Matched Controlled Trial

Guy's and St Thomas' NHS Foundation Trust0 个研究点目标入组 183 人开始时间: 2018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
入组人数
183
主要终点
establishing which appliance has the fastest completion time

研究概览

简要总结

To investigate each treatment modality in its "optimal" environment to avoid operator experience bias. Therefore we propose to operate out of three "specialist centres" with specific units providing one modality alone Which of the three orthodontic appliances does achieve best clinical progress, produce least discomfort to the patient, minimize the time taken for completion of treatment and maximize compliance.

详细描述

Patients and materials: The patient population will consist of patients age 10-16 that have, or are close to having, a full permanent dentition, and present to the clinic with Class II malocclusions with more than 1/2 unit II molar relationship. (Normal or deep overbite cases are also included). The treatments to be compared are the three (routinely-used) orthodontic appliances: Twin Block, Herbst and Frog.

Hypothesis: The principal (null) hypothesis is that there is no difference between the three appliances in terms of their effectiveness, efficiency and compliance.

Study design: The study is designed as a multicentre, Prospective Expertise Based Matched Controlled Longitudinal Trial and the assessments will be longitudinal in time.

All patients that consent/assent to be part of the study (and their parents) will receive an information leaflet about the study and will be asked to sign an assent form. Patients are free to discontinue treatment if they wish to do so. The normal length of orthodontic treatment is between 18 and 24 months. Assessments will be taken prior to treatment and throughout the treatment period, with regular progress reviews every 3 months, as per standard practice.

Outcomes: The principal outcome for efficiency is the time taken for completion of treatment. The principal outcomes for effectiveness are the clinical progress, discomfort (caused by the appliance to the patient) and compliance.

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
10 Years 至 16 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Patients aged 10-16 years of age in the late mixed/permanent dentition with Class II malocclusions (Both Cl II div 1 and Cl II div 2)
  • > 1/2 unit Class II molar relationship bilaterally (at least 3.5mm)
  • Normal or deep overbite cases will be included
  • Skeletal Class II relationship (ANB > 4°)
  • Overjet ≥ 5 mm in Cl II/1 cases
  • Non-extraction cases

排除标准

  • Children in the early mixed dentition
  • Class I and Class III malocclusions
  • Malocclusions with less than 1/2 unit II molar relationship
  • Reduced overbite / anterior openbite
  • Medically compromised patients, syndromic patients or patients with severe facial asymmetry
  • Special needs patients not able to comply with instructions / difficulty with compliance
  • Hypodontia or extracted permanent tooth (except third molars)
  • Poor oral hygiene with both Gingival bleeding Index and Plaque Index scoring no more than 1

研究组 & 干预措施

Twin Block

Experimental

61 patients will receive the Twin Block appliance (one of the three appliances being studied)

干预措施: Twin Block, Herbst, Frog distalising appliance (Device)

Herbst

Active Comparator

61 patients will receive the Herbst appliance (one of the three appliances being studied)

干预措施: Twin Block, Herbst, Frog distalising appliance (Device)

Frog distalising appliance

Active Comparator

61 patients will receive the Frog distalising appliance (one of the three appliances being studied)

干预措施: Twin Block, Herbst, Frog distalising appliance (Device)

结局指标

主要结局

establishing which appliance has the fastest completion time

时间窗: 18-24 months

The three appliances will be compared in 'months' from the start of treatment till the completion of treatment to see which is the fastest to achieve the end result

Number of participants who have experienced discomfort related to wearing the appliance

时间窗: 18-24 months

This is to check which appliance produces more discomfort compared to the other appliances using the Likert scale. Each question on the scale asks to rate the pain as either (no pain, slight pain, moderate pain, severe pain) or (strongly disagree, disagree, agree, strongly agree). Patients will choose a response which matches their experience.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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