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临床试验/CTRI/2024/02/063009
CTRI/2024/02/063009招募中3 期

Comparison of efficacy and safety of Prednisolone 20 mg vs Placebo in Diabetic patients with Complex Regional Pain Syndrome of upper extremity - PPDCRPS

Professor Jayantee Kalita0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
发起方

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

入选标准

  • A) Continuous pain which is disproportionate to any inciting factor.
  • B) At least one symptom in three of the four following domains.
  • 1) Sensory: hyperesthesia with or without allodynia.
  • 2) Vasomotor: Asymmetry in temperature or skin color, skin color changes of the affected limb.
  • 3) Sudomotor/edema: Presence of edema, sweating changes or sweating asymmetry.
  • 4) Motor/ trophic: Reduced range of motion or motor dysfunction with or without trophic changes of the limb.
  • C). At least one sign in = 2 of the following domains.
  • 1) Sensory: Hyperalgesia (to pin prick) with or without allodynia (light touch, deep somatic presence or joint movements).
  • 2) Vasomotor: Evidence of temperature or skin color asymmetry, or skin color changes.
  • 3) Sudomotor/edema: edema, sweating changes or sweating asymmetry.
  • 4) Motor or trophic: Evidence of deduced range of movement, motor dysfunction (weakness, dystonia or tremor) and or trophic changes in nail, skin or hair.
  • 5) No other diagnosis could explain the symptoms or signs

排除标准

  • Patients with uncontrolled hypertension, diabetes, infection, organ
  • failure, malignancy, shoulder joint dislocation or infection, pregnancy and unwilling for consent will be excluded

研究者

发起方
Professor Jayantee Kalita

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