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临床试验/NCT01657149
NCT01657149终止不适用

Influence of Manual Lymph Drainage During Hospitalization on Swelling, Function and Pain in Patients After Total Knee Replacement - Randomized Control Trial.

Rabin Medical Center1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2015年12月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
20
试验地点
1
主要终点
Circumferential measurement of limb volume

研究概览

简要总结

To investigate the effects of lymphatic drainage massage performed immediately after total knee replacement in relation to reduction of limb circumference, pain reduction and functional improvement.

详细描述

In the past few decades there has been a rise in the number of knee replacements performed due to degenerative arthritis. In general over the years the number of operations has risen while the age of the patients has gone down. The aim of these operations is to improve quality of life, alleviate pain and improve function.

Post operative complications can delay recovery and rehabilitation, lengthen hospitalization duration and in extreme cases lead to failure of the operation. These complications include infection, deep vein thrombosis, swelling and edema, pain, impairment of range of motion, muscle weakness and functional disability.

Reduction of post operative edema may help to speed up recovery after total knee replacement.

Recently an effective treatment has been found for lymphatic edema that appears after oncological operations that include removal of lymph nodes or due to blood vessel disorders. This treatment is administered by a physiotherapist and includes lymphatic drainage massage, compression bandaging and exercises.

This trial will examine the effect of lymphatic massage treatment on orthopedic patients to ascertain if the use of this technique can shorten the duration and improve the quality of the post operative rehabilitation and prevent other post operative complications. At the present time not enough research has been done in this field and it is necessary to continue to investigate the efficiency of the lymphatic treatment in acute orthopedic patients.

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
Single (Outcomes Assessor)

入排标准

年龄范围
50 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • primary total knee replacement
  • ages 50-85
  • preserved cognitive facilities and comprehension.

排除标准

  • Severe chronic heart failure.
  • previous episode of lymph edema.
  • surgical removal of lymph nodes in the lower limbs.
  • significant scarring of the lower limbs (larger than 10 cm).
  • Deterioration in a patient's medical condition or an infection of the lower limb during the trial period will also cause exclusion of that patient.

结局指标

主要结局

Circumferential measurement of limb volume

时间窗: The circumferential measurements will be assesed pre operative and post operative on daily basis for 5 days post op

次要结局

  • Visual Analogue Scale (VAS) Inclinometer(VAS & INCLINOMETER will be assessed on a daily basis for 5 days post op)
  • Daily functional capacity Assessment(Daily functional capacity Assessment after 6 days post op. All Outcomes will be reassessed after 6 weeks post op)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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