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临床试验/ACTRN12612000260820
ACTRN12612000260820尚未招募未知

Randomised controlled trial comparing ultrasound-guided to patient-guided extracorporeal shock wave therapy (ESWT) for calcific soft tissue pathologies (including tendinopathy) when assessing patient outcomes of decreased pain, improved function and reduced calcification size.

Dr John Orchard0 个研究点目标入组 120 人开始时间: 2012年3月2日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
120

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
Open (masking not used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Pain in one of 3 areas - either shoulder rotator cuff tendon, achilles tendon or plantar fascia; Proven calcification visible on previous imaging;Calcification visible on our ( the investigator's) ultrasound machine; Males and non-pregnant females; fluent in english; able to give informed consent; seeking to try shockwave treatment as a method to resolve the pain; willing and able to follow the research protocol

排除标准

  • Calcification unable to be seen on our ( the investigator's) ultrasound machine; unable to follow the protocol; unable to tolerate the shock wave treatment according to the protocol because it is too painful; corticosteriod injection to the area inthe last 3 months ( as this may affect treatment efficacy); pregnancy or suspected pregnancy during the study; cancer; local lesions or non-intact skin; osteoarthritis at treatment site; Polyneuropathy; bleeding or clotting conditions; anticoagulation medications; allergy to ultrasound gel.

研究者

发起方
Dr John Orchard

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