A Prospective, Randomised Control Trial Investigating the Use of a Two-layer, Short-stretch Compression Bandage in Elective Total Knee Replacement - Feasibility
试验速览
- 阶段
- 不适用
- 入组人数
- 50
- 试验地点
- 3
- 主要终点
- Feasibility
研究概览
简要总结
The use of compression bandages in elective orthopaedic knee surgery is well regarded, however, there is a lack of robust, well-designed evidence to support this.
The aim is to determine the feasibility of conducting a randomised control trial comparing the use of a compression bandage worn post-operatively for 24 hours after elective total knee replacement, compared to standard practice (wool and crepe, non-compressive dressing).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Age > 18
- •Able to give written, informed consent
- •Primary total knee replacement
排除标准
- •Extensive peripheral vascular disease
- •Lower limb neurological disorder
结局指标
主要结局
Feasibility
时间窗: 6 months
Additionally, the study is a feasibility study to estimate (via the pilot trial) rates of patient recruitment, randomisation, retention and response, logistics of trial methodology, and resource utilisation.
次要结局
- Pain(6 months)
- Patient satisfaction(6 months)
- Knee range of motion(6 months)
研究者
Mike Reed
Consultant Trauma and Orthopaedic Surgeon
Northumbria Healthcare NHS Foundation Trust