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临床试验/PER-063-02
PER-063-02已完成未知

MULTICENTER, RANDOMIZED, DOUBLE-BLIND STUDY OF PARALLEL GROUPS, TO COMPARE THE EFFECTIVENESS AND TOLERABILITY OF VALDECOXIB VS. DICLOFENACO IN THE ANKLE SPLINT

PHARMACIA & UPJOHN INTERAMERICAN CORPORATION,0 个研究点目标入组 0 人开始时间: 2002年10月28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

  • Men or women> 18 years old with the legal age required to grant their consent.
  • Women who are postmenopausal or surgically sterilized, or who have had a urine pregnancy test with a negative result before randomization.Men or women> 18 years old with the legal age required to grant their consent.
  • Women who are postmenopausal or surgically sterilized, or who have had a urine pregnancy test with a negative result before randomization.

排除标准

  • Clinical evidence of complete rupture of the ligaments of the ankle
  • (sprain of third degree).
  • Requires bed rest, hospitalization, surgical intervention to
  • ankle injury or complete non-removable cast of any kind.
  • presence of bilateral ankle injury or ipsilateral ankle injury and
  • A similar injury to the same joint suffered in the last six

研究者

发起方
PHARMACIA & UPJOHN INTERAMERICAN CORPORATION,

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