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临床试验/ISRCTN36315634
ISRCTN36315634已完成不适用

Mannitol to prevent an exacerbation of Complex Regional Pain Syndrome (CRPS) after hand surgery

niversity Medical Centre Utrecht (UMCU) (Netherlands)0 个研究点目标入组 50 人开始时间: 2006年1月27日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Age at least 18 years
  • 2. History of CRPS, indicated by the presence of the following characteristics during the past 3 years (adapted CRPS I criteria according to Bruehl):
  • 2.1. Continuing pain, disproportionate to any inciting event
  • 2.2. At least 1 symptom in one of the following 4 categories:
  • 2.2.1. Sensory: hyperalgesia
  • 2.2.2. Vasomotor: temperature asymmetry or skin color changes or skin color asymmetry
  • 2.2.3. Sudomotor/edema: edema or sweating changes or sweating asymmetry
  • 2.2.4. Motor/trophic: diminished range of motion or motor dysfunction or trophic changes
  • 3. The presence of CRPS signs is not mandatory
  • 4. Surgery on the affected upper extremity (a.o. carpal-tunnel syndrome, joint surgery on wrist and fingers)

排除标准

  • 1. Allergy to mannitol
  • 2. Allergy to hydrochlorothiazide
  • 3. Clinically relevant renal impairment (creatinine =150% normal)
  • 4. History of cardiac failure (orthopnea, edema, exertional dyspnea, admissions for cardiac failure)
  • 5. CRPS in both upper extremities
  • 6. Other pain syndromes affecting functional testing or pain scores
  • 7. Infection
  • 8. Pregnancy
  • 9. No informed consent

研究者

发起方
niversity Medical Centre Utrecht (UMCU) (Netherlands)

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