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临床试验/NCT05904587
NCT05904587招募中不适用

Clinical Evaluation of the Effectiveness of Different Methods in Reducing Pain During Debonding of Orthodontic Fixed Appliance: a Randomized Clinical Trial

University of Baghdad2 个研究点 分布在 1 个国家目标入组 128 人开始时间: 2023年3月19日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
128
试验地点
2
主要终点
pain during debonding of conventional fixed orthodontic appliance

研究概览

简要总结

The goal of this clinical trial is to evaluate the effectiveness of four different methods (including the control group) in reducing pain during debonding of fixed orthodontic appliances in participants requiring the removal of their fixed orthodontic appliance.

The main question it aims to answer is which method (biting on a cotton roll, biting on a soft thermoplastic elastomeric sheet, and the use of low-level vibration in reducing pain during the debonding procedure) is most effective in reducing the patients' pain during debonding of conventional orthodontic fixed appliances.

Participants will be asked to give their pain score on a scale of 0 to 100 VAS (visual analogue scale) for every region of the dentition.

the researcher then will compare different scores of different methods to find the most effective method in reducing pain.

详细描述

After signing the consent form, the patient will be tested using General Anxiety Disorder 7 (GAD-7) to reduce the effect of general anxiety on pain scores. GAD consists of 7 statements designed to measure anxiety. This will aid in identifying individuals who have severe anxiety disorder and exclude them from the study to ensure more accurate results.

Four debonding methods will be used in this study; Routine mechanical debonding with debonding plier with an open mouth, which will be used as control, and three other interventions to manage pain including biting on a cotton roll, biting on an elastomeric wafer, and using vibration. All of the procedures will be done with the archwire in situ and with minimal torsional force on the bracket.

For the control group, the debonding will be done with an open-mouth technique without any support applied to the teeth. The cotton roll method will be done by asking the patient to bite on the cotton roll firmly but not excessively during the debonding procedure.

As for the elastomeric wafer group the patient will bite on the wafer firmly during the debonding procedure, in a similar fashion the patient will bite on the mouthpiece of the VPro vibration device.

Pain will be estimated by using 100mm VAS and recording the results for each sextant, accompanied by the GAD-7 results and the patient's age and gender.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

入排标准

年龄范围
15 Years 至 30 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Patients between 15-30 years of age who could understand, assess, and answer the questionnaires.
  • No history of taking medicine periodically or in the last 24 hours (e.g., painkillers, corticosteroids, and anti-flu drugs).
  • No debonded brackets prior to debonding procedure.
  • No missing teeth except extracted premolar.
  • Undergoing upper and lower fixed orthodontic treatment with 0.022-inch metal brackets.
  • Finishing arch wires present for at least two months.
  • No craniofacial deformities that would affect the dentoalveolar bone quality (e.g., cleft lip and palate) .

排除标准

  • History of taking medicine periodically or in the last 24 h (e.g., analgesic, anti-inflammatory and anxiolytic).
  • GAD-7 score of ˃
  • Debonded brackets at the time of debonding.
  • Missing teeth except for extracted premolars.
  • Active periodontal problems (recession and mobility greater than Grade I),
  • Heavily restored or root canal treated tooth.
  • Craniofacial deformities that would affect dentoalveolar bone quality (e.g., cleft lip and palate).
  • Surgical treatment (including impacted tooth removal) and presence of mini-screws.
  • excessive gingival overgrowth.

结局指标

主要结局

pain during debonding of conventional fixed orthodontic appliance

时间窗: Intraprocedural

pain will be estimated using 0-100 VAS (visual analogue scale) of each segment of the dentition during the debonding procedure

次要结局

  • the dentition segment with the highest pain scores(Intraprocedural)

研究者

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

Alhasan Ibraheem Ali

B.D.S.

University of Baghdad

研究点 (2)

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