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临床试验/ACTRN12614000249651
ACTRN12614000249651尚未招募2 期

A single blinded randomised controlled trial to determine the clinical effect size and client concordance following eight weeks using a portable electrostimulation device among people with an active leg ulcer who do not tolerate moderate to high compression therapy

BodyFlow International Pty Ltd0 个研究点目标入组 30 人开始时间: 2014年3月10日最近更新:
适应症

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • 1. Client has an existing leg ulcer with either primary venous or lymphedema as its primary aetiology
  • 2. Client is appropriate for, and the best practice treatment would involve the highest compression therapy available (+40mmHg)
  • 3. Client is currently using (1) no compression therapy or (2) low compression therapy (less than 18mmHg)
  • 4. Client has received wound care education specifically promoting the use of compression therapy
  • 5. The client or carer/legal guardian is able to provide informed consent to participate in the study
  • 6. Client has had a Doppler ultrasound in the last 12 weeks
  • 7. Ankle Pressure Brachial Index is between greater than or equal to 0.8 and less than or equal to 1.2

排除标准

  • 1. Client is using moderate or high compression therapy (equal to or greater than 18mmHg) for any period of the day for one or more days of the week.
  • 2. Client is unable to or does not have someone who can physically implement the Electrostimulation Therapy.
  • 3. Client is unable to or does not have someone who can take low compression garments (for those currently wearing compression) on and off in between Electrostimulation Therapy treatments
  • 4. Client has an existing diagnosis of Deep Vein Thrombosis (DVT)
  • 5. Client has an implanted cardiac device such as a permanent pace-maker or internal defibrillator
  • 6. Diagnosed with an active malignant disease
  • 7. Client is pregnant
  • 8. Client has signs of clinical infection in their ulcer
  • 9. Client has a known reaction to adhesive chemicals such as those used on dressings
  • 10. Client is assessed by their clinician as having fragile skin that is at risk of damage when removing the adhesive pads
  • 11. Client has one of the following medical diagnoses: hypothyroidism, hyperthyroidism, congestive cardiac failure, or hypertension

研究者

发起方
BodyFlow International Pty Ltd

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