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临床试验/NCT05457686
NCT05457686已完成不适用

The Efficacy of Kinesiology Taping After Total Knee Arthroplasty Surgery

Kirsehir Ahi Evran Universitesi2 个研究点 分布在 2 个国家目标入组 187 人开始时间: 2022年7月14日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
187
试验地点
2
主要终点
edema

研究概览

简要总结

In this prospective, randomized controlled trial; To evaluate the effect of kinesiology taping applied for edema on pain, edema and functions in the early period after total knee replacement.Patients who underwent total knee replacement will be included in the 10-day follow-up study.Patients will be divided into three groups by randomization. A conservative postoperative physiotherapy program, which is routinely applied to all groups, will be applied. Thus, no patient will be left without treatment. The first group will be considered as the control group, which will be given only a conservative physiotherapy program.

In addition to the conservative postoperative physiotherapy program, the 2nd group will be taped without applying tension with a plaster and will be considered as the sham group.

In the third group, in addition to the conservative postoperative physiotherapy program, kinesiotaping for payment will be applied.

详细描述

Patients will be divided into three groups by randomization. A conservative postoperative physiotherapy program, which is routinely applied to all groups, will be applied. Thus, no patient will be left without treatment. The first group will be considered as the control group, which will be given only a conservative physiotherapy program.

In addition to the conservative postoperative physiotherapy program, the 2nd group will be taped without applying tension with a plaster and will be considered as the sham group.

In the third group, in addition to the conservative postoperative physiotherapy program, kinesiotaping for payment will be applied.

It is planned to prevent bias between the groups by giving standard analgesic treatment to all three groups in the postoperative period. In the postoperative period, Paracetamol 10 mg/ml Infusion 3*1, 100 mg tramadol hydrochloride tablet 2*1 and celecoxib capsule 100 mg 2*1 will be routinely administered until the discharge period.

Conservative postoperative physiotherapy program:

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
Double (Participant, Outcomes Assessor)

盲法说明

This study was designed as blinded, randomized and controlled.the person who evaluates the patients before and after the treatment is blind.In other words,the person evaluating the patients and the person giving the treatment are different.

入排标准

年龄范围
40 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Performing total knee joint arthroplasty due to stage 4 gonarthrosis
  • Agree to participate in the study
  • Having signed the informed consent form

排除标准

  • Presence of malignancy, infection, rheumatological disease
  • Having a tape allergy
  • Having a diagnosis of lymphedema

结局指标

主要结局

edema

时间窗: 10 days after surgery

thigh, knee and leg diameter measurements to be measured with a tape measure

次要结局

  • Pain Intensity(10 days after surgery)

研究者

发起方
Kirsehir Ahi Evran Universitesi
申办方类型
Other
责任方
Principal Investigator
主要研究者

Mehmet Fevzi Cakmak

assistant proffesor

Kirsehir Ahi Evran Universitesi

研究点 (2)

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