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临床试验/CTRI/2013/07/003817
CTRI/2013/07/003817已完成4 期

A multicentric, prospective, observational Registry for assessment of clinical outcomes in Indian adult (more than 18 years of age), 18-50 and more than 65 years inpatients undergoing surgery more than 2 hrs duration during Suprane anaesthesia - RISE

Baxter India Pvt Ltd0 个研究点目标入组 400 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
400

研究概览

简要总结

暂无简介。

研究设计

研究类型
Pms

入排标准

入选标准

  • (1)Male or female (non-pregnant, non-lactating) who is > 18 years of age, either 18-50 years or >65 years
  • (2)Are American Society of Anesthesiologists physical status of I, II, or III
  • (3)Scheduled to receive desflurane as the general anesthetic for a surgical procedure with an anticipated duration of 120 minutes or longer
  • (4)Expected to be transferred to the PACU after surgery or Planned extubation in operative room
  • (5)Has provided written informed consent (unless the responsible IRB/IEC has granted a waiver of the requirement for informed consent

排除标准

  • (1)Age group 51-64 years of age. Known or suspected genetic susceptibility to malignant hyperthermia
  • (2)Patient in whom general anesthesia is contraindicated
  • (3)Known sensitivity to desflurane or to other halogenated agents
  • (4)Patients who are pregnant or lactating

研究者

发起方
Baxter India Pvt Ltd

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