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临床试验/NCT03326544
NCT03326544已完成不适用

Ultra-sound Guided Saphenous Nerve Block Versus Platelet Rich Plasma for Chronic Knee Joint Osteoarthritis

Mansoura University2 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2017年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
56
试验地点
2
主要终点
Pain scores

研究概览

简要总结

Knee osteoarthritis, as a progressive disease is one of the most common causes of pain, motor disorder and disability in the elderly. By increasing age, the cartilage is eroded and endures degenerative changes due to physiological and biomechanical changes as well as metabolic effects and trauma . Non-surgical interventions for pain control of knee osteoarthritis include weight loss, exercise, changes in daily activities, physiotherapy, nonsteroidal anti-inflammatory drugs (NSAIDs) and analgesics .However ,the intra-articular injection is recently recommended by many studies such as corticosteroids, hyaluronic acid, Growth hormone, dextrose ,and platelet rich plasma.

Intra-articular injection of platelets are activated and undergo degranulation, releasing a range of growth factors, including transforming growth factor beta (TGF-β), platelet-derived growth factor (PDGF), insulin-like growth factor, vascular endothelial growth factors, epidermal growth factors and basic fibroblast growth factor 2. These growth factors are thought to activate a variety of signaling pathways, which promote healing of bone and soft tissue.Also,some minimally invasive therapeutic options have been effective in pain relieve in KA, such as ultrasound-guided saphenous nerve block .

详细描述

The aim of this study is to compare the efficacy of ultrasound guided saphenous nerve block versus platelet rich plasma injection in the management of chronic pain in patients with knee OA. This study will be conducted to evaluate which modality is more effective.

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
Single (Participant)

入排标准

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

入选标准

  • Patients who are not competent to understand the study protocol
  • Radiographic evidence of OA of knee of 2nd degree.
  • Chronic pain for at least 6 months prior to study entry (day 0).
  • Pain relief not achieved with conservative therapies during the last 6 months

排除标准

  • Patient refusal.
  • Bleeding disorders.
  • Coagulation disorders.
  • Local skin infection
  • Current other problem in the affected extremity .
  • Psychiatric disorders affecting co-operation of the patient .
  • Previous chronic opioid use.
  • Intra articular knee injection within previous three months.
  • History of traumatic arthropathy.
  • History of neuropathic arthropathy.
  • Allergy or hypersensitivity to any of the study medication.
  • Any condition that could interfere with the interpretation of the outcome assessments.
  • Pregnancy
  • Lactating women.
  • low back pain due to central cause.

结局指标

主要结局

Pain scores

时间窗: For 6 months after intervention

The severity of pain will be assessed using a visual analog scale (VAS)

次要结局

  • Quality of life (QOL)(For 6 months after intervention)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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