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临床试验/JPRN-UMIN000005142
JPRN-UMIN000005142已完成4 期

COMPARATIVE STUDY OF SINGLE-DOSE AND THREE-DAY THERAPY FOR LAPAROSCOPIC CHOLECYSTECTOMY - COMPARATIVE STUDY OF SINGLE-DOSE AND THREE-DAY THERAPY FOR LAPAROSCOPIC CHOLECYSTECTOMY

Kyoto Prefectural University of Medicine Division of Digestive Surgery, Department of Surgery0 个研究点目标入组 50 人开始时间: 2011年2月25日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
50

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
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • Patients have been treated with other antibiotics before the start of study drug administration Patients were treated with quinolone antibacterial agent within one week before the start of study drug administration Treatment with oral administration in patients with severe infection is not expected to effect Complications have serious underlying disease, patients have difficulty assessing the safety and efficacy of drug testing Patients with a history of allergy to quinolone antibacterials Patients with Severe cardiac dysfunction, liver dysfunction Patients with severe renal impairment Patients with a history of epilepsy or other seizure disorder Pregnant women and lactating women and the women are pregnant may Patients who are considered unsuitable for the doctor

研究者

发起方
Kyoto Prefectural University of Medicine Division of Digestive Surgery, Department of Surgery

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