ISRCTN39292293已完成Unknown
Quality of life, physical activity and satisfaction of patients after intra-articular injection of hyaluronic acid with mobile reticulum for the treatment of chondral injury of the knee due to osteoarthritis due to overuse and/or in the conservative treatment of the meniscus injury
Centre de Tecnificació Esportiva de la Residencia Blume0 个研究点目标入组 165 人开始时间: 2023年5月11日最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- 入组人数
- 165
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 性别
- All
入选标准
- •The study population comprised patients (male or female) older than 18 years seen at one of the participating clinics between December 2018 and July 2019 for their first follow-up visit after intra-articular injection of mobile reticulum hyaluronic acid due to:
- •1. Mild to moderate symptomatic knee osteoarthritis responding to clinical and radiological criteria of American College of Rheumatology (ACR) and a Kallgren and Lawrence (KL) score II/III evidenced by radiography and/or MRI. Patients received two consecutive intra-articular injections of HYMOVIS (3 ml syringe with 8 mg of non-cross-linked HA alkylamida HYADD4; FIDIA Farmaceutici, Italy) given at 1-week intervals according to the prospect.
- •2. Knee meniscal tear (traumatic or degenerative) objectifiable by radiography and/or MRI. Patients received two consecutive intra-articular injections of HYMOVIS given at 2-week intervals according to the prospect.
- •3. Mild to moderate symptomatic knee osteoarthritis with meniscal tear. Patients received two consecutive intra-articular injections of HYMOVIS given at 1-week intervals according to the prospect.
排除标准
- •1. Viscosupplementation or corticosteroid therapy in the last 6 months
- •2. Concomitant diseases that could interfere with the tests during the data collection period or that could lead to erroneous results (i.e., rheumatoid arthritis, metabolic bone diseases, gout, Paget's disease of bone, symptomatic chondrocalcinosis)
- •3. Knee arthroplasty or other knee surgery in the last 12 months
- •4. Any scheduled surgery during the data collection period
- •5. Evidence or suspicion of infection in the affected joint or skin diseases of the knee, such as dermatitis or psoriasis
- •6. Patients with bilateral knee OA
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