跳至主要内容
临床试验/NCT06967246
NCT06967246已完成不适用

Effect of Kinesio Taping of Pain, Swelling and Trismus After Mandibular Third Molar Surgery

University of Medicine and Pharmacy at Ho Chi Minh City2 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2023年9月1日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
17
试验地点
2
主要终点
post operative pain

研究概览

简要总结

This study evaluates the effectiveness of kinesio taping in reducing swelling, pain, and trismus complications after wisdom tooth extraction surgery. Patients undergoing bilateral symmetrical extraction of mandibular third molars, Kinesio tape was applied on the study side and placebo tape on the control side. Pain intensity was assessed using the Visual Analog Scale (VAS), swelling was measured using predefined facial landmarks, and mouth opening was recorded using interincisal distance measurements. Data were collected preoperatively (T0) and on the 1st (T1), 2nd (T2), and 3rd (T3) postoperative days.

详细描述

Introduction

Complications following third molar surgery can affect patients' quality of life. Kinesio taping is a simple, non-invasive method with a clear mechanism of action in fluid drainage, one of the strategies for symptom reduction in wisdom tooth extraction surgery. This study evaluates the effectiveness of kinesio taping in reducing swelling, pain, and trismus complications after wisdom tooth extraction surgery.

Methods: A split-mouth, randomized, placebo-controlled clinical trial was conducted on 17 patients indicated bilateral mandibular third molar extraction. Each patient had Kinesio tape applied to one surgical site and a placebo tape to the contralateral side. Pain intensity was assessed using the Visual Analog Scale (VAS), swelling was measured using predefined facial landmarks, and mouth opening was recorded using interincisal distance measurements. Data were collected preoperatively (T0) and on the 1st (T1), 2nd (T2), and 3rd (T3) postoperative days.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Supportive Care
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients have bilaterally impacted mandibular third molars that are relatively symmetrical and have the same difficulty according to Pell and Gregory's classification, with an angulation difference between the two teeth not exceeding 15°. The angulation of each third molar is measured on a panoramic X-ray as the angle formed between the long axis of the third molar and the adjacent second molar.
  • Patients do not have preoperative symptoms of swelling or pain.
  • Patients agree to participate in the study after receiving a clear explanation and counseling.

排除标准

  • Patients with systemic conditions contraindicating tooth extraction surgery.

结局指标

主要结局

post operative pain

时间窗: 1st, 2nd, 3rd post operative days

* Pain intensity was evaluated using the Visual Analog Scale (VAS) and the total number of analgesic tablets consumed by the patient. Patients self-assessed their pain levels using VAS during the first 3 days after surgery. * The VAS is a 100 mm long straight segment from 0 (painless) to 100 (unbearable pain).

post operative swelling

时间窗: 1st, 2nd, 3td postoperative day

- Preoperative facial measurements were recorded by assessing the lengths of the following segments: * AB (vertical dimension): From the outer canthus (A) to the lowest point of the mandibular angle (B). * CD line (horizontal dimension): from the midpoint of the tragus (C) to the oral commissure (D). * BD line (oblique dimension): from the lowest point of the mandibular angle (B) to the oral commissure (D). On each assessment timepoint: - The patient sat in a 45-degree reclined chair position with the lower jaw in the resting position. Swelling was assessed by re-measuring 3 segments: AB, CD and BD during the first 3 days after surgery.

次要结局

  • Number of painkiller tablets:(1st, 2nd, 3rd post operative days)
  • post operative trismus(1st, 2nd, 3td postoperative day)

研究者

发起方
University of Medicine and Pharmacy at Ho Chi Minh City
申办方类型
Other
责任方
Principal Investigator
主要研究者

Lam Cu Phong

lecturer, clinical professor

University of Medicine and Pharmacy at Ho Chi Minh City

研究点 (2)

Loading locations...

相似试验