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临床试验/NCT07333963
NCT07333963已完成不适用

Application of Kinesiotaping as an Adjunctive Physiotherapeutic Method in the Surgical Management of Impacted Mandibular Third Molars

Medical University of Silesia1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2023年5月14日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
70
试验地点
1
主要终点
postoperative pain intensity

研究概览

简要总结

PATIENT INFORMATION SHEET Participants are invited to take part in a clinical study involving surgical removal of an impacted lower wisdom tooth. Participation in this study is entirely voluntary.

The purpose of this study is to observe the healing process after wisdom tooth removal and to assess whether the use of elastic therapeutic tape placed on the skin (kinesiotaping) may support recovery.

SURGICAL PROCEDURE The procedure will be performed under local anesthesia and will include: - Administration of local anesthesia

  • Incision of the gum
  • Exposure of the impacted tooth and surrounding bone
  • Removal of the tooth
  • Cleaning of the surgical site - Placement of sutures After the surgery, standard post■operative instructions will be provided. STUDY PROCEDURE

After the surgical procedure, patients will be randomly assigned to one of two groups:

  1. Standard post■operative care
  2. Post■operative care combined with application of elastic therapeutic tape on the skin of the face and neck area If the participants are assigned to the tape group, the tape will be applied immediately after surgery by qualified medical personnel and will remain in place for several days.

FOLLOW■UP VISITS Participant will be asked to attend follow■up visits on specific days after the procedure to allow the medical team to assess healing. PAIN MANAGEMENT Participant will be allowed to take pain medication if necessary, following medical advice.

VOLUNTARY PARTICIPATION Participation in this study is voluntary. Participant may withdraw from the study at any time without giving a reason and without affecting participants medical care.

CONFIDENTIALITY All medical information collected during the study will be handled confidentially and used solely for research purposes.

研究设计

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

入排标准

年龄范围
16 Years 至 64 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • No systemic diseases (generally healthy patient)
  • Indication for surgical extraction of impacted lower third molars for:
  • orthodontic reasons
  • surgical reasons
  • prophylactic reasons
  • Age between 16 and 64 years
  • Written informed consent to participate in the study

排除标准

  • Presence of chronic systemic diseases, including:
  • diabetes mellitus
  • hypertension
  • autoimmune diseases
  • Pharmacological treatment in the period preceding the surgery
  • Substance abuse or dependence
  • Head and neck malignancies

研究组 & 干预措施

Control Group

Other

no kinesiotaping

干预措施: extraction of impacted third lower molar (Procedure)

Research group

Experimental

Group undergoing Kinesiotaping after the surgical procedure

干预措施: Kinesiotaping (Other)

Research group

Experimental

Group undergoing Kinesiotaping after the surgical procedure

干预措施: extraction of impacted third lower molar (Procedure)

结局指标

主要结局

postoperative pain intensity

时间窗: 2 days post-surgery and 7 days post-surgery

Postoperative pain intensity will be assessed using the Visual Analog Scale (VAS), ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst pain imaginable. Higher scores indicate greater pain intensity.

Facial Soft Tissue Swelling

时间窗: Before surgery, 2 days after surgery, and 7 days after surgery

Facial swelling will be assessed using linear tape measurements between six predefined facial reference points. The sum of distances will be used for analysis.

Maximum Mouth Opening (MMO)

时间窗: FinishBefore surgery, 2 days after surgery, and 7 days after surgery

Maximum mouth opening will be measured using a caliper as the interincisal distance between the upper and lower incisors at maximum mouth opening.

Postoperative Analgesic Consumption

时间窗: Day of surgery, 2 days after surgery, and 7 days after surgery

The total number of ketoprofen 100 mg tablets taken by each participant will be recorded as a measure of postoperative analgesic demand.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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