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临床试验/IRCT201303135393N2
IRCT201303135393N2已完成未知

Propofol or sodium thiopental in patients undergoing reproductive assisted technologies: comparative efficacy in hemodynamic recovery from anesthesia and outcome of oocyte retrieval

Yazd University of medical sciences0 个研究点目标入组 90 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
90

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
20 years 至 35 years(—)
性别
Female

入选标准

  • (inclusion criteria: lack of infertility problems in the women and the presence of fertility problems in their husbands; Informed consent)
  • (Exclusion criteria: History of Hypertension; chronic respiratory diseases; thyroid disorders; severe side effects of drugs during the experiment)

排除标准

  • 未提供

研究者

发起方
Yazd University of medical sciences

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