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临床试验/IRCT20230204057318N3
IRCT20230204057318N3招募中3 期

Comparison of multimodal analgesia and opioid based method in urethral reconstruction surgery

Shahid Beheshti University of Medical Sciences0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
30

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
18 years 至 no limit(—)
性别
Male

入选标准

  • Patient candidate for urethral reconstruction treatment
  • Mental health and providing informed consent
  • Ability to adhere to patient visit schedule and other relevant protocols
  • American Society of Anesthesiologist (ASA) score I or II
  • Normal kidney and liver function

排除标准

  • Any condition that prevents obtaining informed consent.
  • Any other disease, including malignancy, abnormal laboratory tests, psychiatric disease, which in the opinion of the researcher prevents the patient from adhering to the study.
  • Concomitant or uncontrolled illness that, in the researcher's opinion, causes harm to the patient or non-adherence to the study.
  • History of drug addiction, psychoactive drugs and other illegal drug substances

研究者

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