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临床试验/PER-049-02
PER-049-02已完成未知

DOUBLE BLIND STUDY PARALLEL RANDOMIZED AND ACTIVE COMPARATOR WHOSE PURPOSE IS TO EVALUATE THE SAFETY AND EFFICACY OF CELECOXIB IN SUSPENSION COMPARED WITH NAPROXEN IN SUSPENSION IN PATIENTS WITH YOUNG RHEUMATOID ARTHRITIS.

PHARMACIA & UPJOHN INTERAMERICAN CORPORATION,0 个研究点目标入组 0 人开始时间: 2002年7月22日最近更新:

试验速览

阶段
未知
状态
已完成
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

  • 1. The patient has a diagnosis of JRA of a polyarticular or oligoarticular course determined according to the CAR criteria. Patients with systemic onset JRA who have a polyarticular or oligoarticular course are eligible. Patients with Active systemic characteristics will not be included.
  • 2. The patient is at least two years old and has not yet reached his 17th birthday.
  • 3. The patient must weigh at least 15 kg.
  • 4. The patient must have> 1 swollen joint and> 1 joint with limitation of the movement. Joints with limited range of movements can be the same as the swollen joints.
  • 5. Must have rm CESN score of> 0.2.
  • 6. Must have a global evaluation by the physician and the father in the selection of> 20 mm on a 100 mm EVA scale.

排除标准

  • 1. The patient is in the active phase of systemic JRA.
  • 2. The patient has received or has been exposed to investigational drugs within the specified times before receiving the first dose of the medication.

研究者

发起方
PHARMACIA & UPJOHN INTERAMERICAN CORPORATION,

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