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临床试验/NCT05291793
NCT05291793已完成不适用

The Effect of Different Intra-articular Injections on Pain and Function in Primary Gonarthrosis

Nevsehir Haci Bektas Veli University3 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2020年4月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
80
试验地点
3
主要终点
Visual Analogue Scale (VAS)

研究概览

简要总结

Gonarthrosis is a frequent cause of knee pain and mostly related to altered function of the knee. Intra-articular injections are a valuable noninvasive medical treatment of choice for pain management and functional enhancement. This study aims to investigate the effects of intra-articular injections without local anesthesics which are well known to be chondrotoxic. For this purpose, functional data of the patients who received intra-articular injections have been collected and analyzed.

详细描述

Intra-articular knee injections are commonly used treatment method. It is preferred to relieve the pain and functional limitation due to knee osteoarthritis. Studies have shown the benefit of intra-articular injections, including intra-articular sterile saline injection alone. In addition, studies have shown chondrotoxic effects of local anesthetics and corticosteroids such as triamcinolone. Local anesthetics are often added to the injection in intra-knee injections. Many previous studies stated that anesthetic agents were mixed with corticosteroid and NSAID intra-articular injections but not in this study. This creates confusion on which preparation is effective on pain and function. The aim of this study is to compare pain-reducing and function-improving effects of intra-articular injection with corticosteroids or NSAIDs, while avoiding local anesthetics whose chondrotoxic effects have been confirmed. In order to reveal the unmasked effect, an intra-articular saline injection group was introduced as a sham treatment. Thus, a study with a level of evidence 1 will make a significant contribution to the literature.

Patients who applied to the outpatient clinic and who were diagnosed with primary gonarthrosis by clinical and radiographic examinations have been randomized to four different groups by closed-envelope method following taking the informed consent. Accordingly, nonsteroidal anti-inflammatory (NSAI) drugs have been prescribed to all diagnosed patients. Demographic data of the patients have been noted and randomized into four equal groups of thirty individuals each. Afterwards, the first group received NSAID treatment, the second group received intra-articular methylprednisolone, the third group received intraarticular tenoxicam, and the fourth group received intra-articular sterile saline injection. All eligible patients have been given one random envelope by the secretary, then proceeded to the injection room with envelopes closed. The orthopedic technician prepared the injection depending on the information inside the envelope then the syringe is covered with opaque plaster or foil. Then, an injection was applied by the physician blindly. The patients' visual analog score(VAS) pain form and WOMAC scores are collected in each follow-up. Following the data has been obtained by an independent data recorder, all data have been saved to the database and statistical results were analyzed. According to the posthoc power analysis, the number of patients can be revised for statistical power.

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, Care Provider)

盲法说明

patients were not aware of the ingredient of the injection they had received Care providers were not aware of the ingredient of injection during application

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 older than 18 years old
  • Diagnosed as Osteoarthritis ( in weight-bearing standing Antero-Posterior and Lateral knee plain radiographs)

排除标准

  • Patients refuse to enroll in the study voluntarily
  • Patients refuse to give informed consent
  • Patients who have received physiotherapy and/or intraarticular injection in the last 6 months.
  • Patients who have used supporting brace treatment in the last 6 months
  • Patients did not attend routine follow-up visits.
  • Patients experienced any allergic reaction to the administered drug

研究组 & 干预措施

Tenoxicam

Active Comparator

Group 2, patients received intraarticular tenoxicam ( 20 mg) once.

干预措施: Tenoxicam 20 Mg Powder for Solution for Injection Vial (Drug)

Methylprednisolone

Active Comparator

Group 3, patients received intraarticular methylprednisolone once(40mg).

干预措施: Methylprednisolone (Drug)

Saline

Sham Comparator

Group 4, patients received an intraarticular sterile saline injection(4ml).

干预措施: Saline (Drug)

结局指标

主要结局

Visual Analogue Scale (VAS)

时间窗: at 6th week following intra-articular injection

Visual Analogue Scale ( Score:0 corresponds to 'no pain', score:10 corresponds to excessive pain)

The Western Ontario and McMaster Universities Arthritis Index (WOMAC)

时间窗: at 6th week following intra-articular injection

The Western Ontario and McMaster Universities Arthritis Index (WOMAC), Score ranges between 0-100, Higher scores represent worse pain and poorer functioning, WOMAC score:0 corresponds to no functional impairment, WOMAC score:100 represents to complete impairment.

次要结局

未报告次要终点

研究者

发起方
Nevsehir Haci Bektas Veli University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Yiğit Umur Cırdı

Medical Doctor, Orthopedics and Traumatolgy Specialist, Principal Investigator

Acibadem Kozyatagi Hospital

研究点 (3)

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