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临床试验/EUCTR2013-000832-85-IT
EUCTR2013-000832-85-IT进行中(未招募)1 期

INTRAMUSCULAR CLODRONATE 200 MG IN THE THERAPY OF HANDS IN PHASE ALGIC OSTEOARTHROSIS - A 6 MONTHS PILOT OPEN STUDY. - ERODE 2

Fondazione Salvatore Maugeri, IRCCS0 个研究点目标入组 60 人开始时间: 2013年8月23日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • ° male and female population over 18 years
  • ° erosive osteoarthritis diagnosed according to international radiological criteria (at least 2 interphalangeal joints in erosive phase) or primary osteoarthritis of the hands diagnosed according to clinical ACR steroid therapy and DMOADs any suspended for at least three months, including infiltration
  • ° phase algic in place to load interphalangeal hands with VAS ? 4 cm/10
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 40
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 20

排除标准

  • ° erosive osteoarthritis and primary osteoarthritis in inactive phase and not algic
  • ° with osteoarthritis of the hands with functional impairment no longer editable (ankylosis)
  • ° patients with digestive diseases that contraindicate the use of NSAIDs
  • ° suffering from kidney disease, cardiovascular and neoplastic
  • ° suffering from systemic diseases and non-severe, not yet stabilized
  • ° suffering from psychiatric and / or neurological relevant
  • ° suffering from rheumatism, fibromyalgia primary or secondary
  • ° syndromes of the upper canalicular
  • ° suffering from chronic inflammatory arthropathy albeit temporarily in remission.
  • ° those who take illegal drugs and / or alcohol in doses which constitute abuse.
  • ° patients with known or suspected hypersensitivity to bisphosphonates
  • ° subjects presenting contraindication to the use of NSAIDs
  • ° subjects not willing to give their informed consent to participation in the study and patients who do not ensure adequate adherence to the study requires.
  • ° patients who are pregnant or nursing, or who have good chance of it during the course of the study.

研究者

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