PER-077-02已完成未知
CLINICAL PROTOCOL FOR A MULTICENTER, DOUBLE-BLIND, RANDOMIZED STUDY OF THE EFFICACY AND SAFETY OF A SINGLE DOSAGE OF PARODOXIB SODIUM IV VS. A SINGLE DOSE OF KETOPROPHENE IV VS. ONE UNIQUE DOSAGE OF KETOROLACO IV VS. PLACEBO FOR THE TREATMENT OF PAIN AFTER A LAPAROSCOPIC COLLECISECTOMY.
PHARMACIA & UPJOHN INTERAMERICAN CORPORATION,0 个研究点目标入组 0 人开始时间: 2002年12月12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
- 年龄范围
- 0 至 0（—）
入选标准
- •1.- Men or women between 18 and 75 years of age.
- •2.- The patient has a body weight of 50 to 120 kg
- •3.- The patient requires an elective laparoscopic cholecystectomy.
- •4.- A procedure is anticipated under an ambulatory patient scheme.
排除标准
- •The patient is scheduled to undergo some other surgical procedure that is expected to produce a greater degree of surgical traction than laparoscopic cholecystectomy alone.
- •Acute preoperative pain other than biliary colic.
- •A condition of chronic pain that requires chronic treatment and / or which, in the opinion of the Investigator, may affect pain assessments or the response to therapy.
- •The patient has any type of cognitive impairment that, in the opinion of the Investigator, would impede participation in the study or adherence to the procedures required in the protocol.
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