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临床试验/NCT07638644
NCT07638644尚未招募不适用

Comparative Efficacy of Acupressure, Ibuprofen, and Chewing Gum in Managing Post-Archwire Orthodontic Pain: A Three-Arm Randomized Clinical Trial

Bahria University0 个研究点目标入组 105 人开始时间: 2026年7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
尚未招募
入组人数
105

研究概览

简要总结

The goal of this clinical trial is to find out which method works best to reduce pain after braces are adjusted for the first time (when the first archwire is placed). The study will compare three approaches: acupressure (applying pressure on a specific point on the hand), ibuprofen (a pain-relief medicine), and chewing sugar-free gum. It will also check how safe these methods are and whether patients need extra pain medicine.

The main questions the researchers want to answer are:

Which method reduces orthodontic pain the most after the first archwire is placed? Do patients need extra painkillers in any of the groups? Are there any problems with braces (such as loose brackets or wire issues) within the first week?

Researchers will compare the three groups to see which option gives the best pain relief during the first few days after braces are activated.

Participants will:

Be placed into one of three groups: acupressure, ibuprofen, or chewing gum Use their assigned method after their first orthodontic wire is placed Rate their pain at different time points using a simple pain scale (VAS) Report if they take any extra pain medicine Be checked for any brace-related problems for up to 7 days

This study may help improve comfort and pain management for patients starting orthodontic treatment.

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)

入排标准

年龄范围
15 Years 至 35 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Age 15 to 35 years
  • Complete permanent dentition
  • Undergoing comprehensive fixed orthodontic treatment
  • Scheduled for initial archwire placement
  • Ability to comply with study procedures
  • Written informed consent provided (or parental/guardian consent for participants younger than 18 years)

排除标准

  • Pregnant or lactating
  • Systemic disorders that may affect pain perception
  • Periodontal disease
  • Neurological abnormalities that may affect pain perception
  • Known sensitivity to chewing gum
  • Documented allergy to ibuprofen
  • Use of adjunctive orthodontic appliances
  • Use of analgesics, anti-inflammatory medications, or other medications that may affect pain perception within 24 hours before enrollment

研究组 & 干预措施

Ibuprofen Intervention

Active Comparator

In the ibuprofen group participants will be provided with a 400 mg oral dose post arch wire placement. With a minimum gap of 8 hours between doses, remaining doses will be taken as per need for the relief of pain with the total daily dose not surpassing 1200 mg.

干预措施: Ibuprofen 400 mg (if necessary) (Drug)

Chewing Gum Intervention

Experimental

Instructions to chew sugar-free gum for a period of 10 minutes immediately post arch wire placement will be provided to the chewing gum group, 8 hourly, for pain relief.

干预措施: Chewing Gum (Behavioral)

Acupressure Intervention

Experimental

Participants in this arm will receive instructions on the use of acupressure for orthodontic pain management following placement of the initial archwire. Verbal instructions and a standardized advice sheet will be provided. Participants will be trained to apply steady, perpendicular pressure using the thumb of the opposite hand to the LI4 (Hegu) acupressure point for approximately 3 minutes. The location of the LI4 point will be demonstrated and identified as the point on the dorsum of the hand between the first and second metacarpal bones, at the midpoint of the second metacarpal bone near its radial border. Participants will be instructed to perform acupressure according to the standardized study protocol.

干预措施: Acupressure (Behavioral)

研究者

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

Shumaila Maryum

Principal Investigator

Bahria University

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