JPRN-jRCT1032210192已完成3 期
Comparison between a conventional method and the use of an automated cuff pressure controller device in the effective sealing pressure: a randomized controlled study.
Okuda Yasuhisa0 个研究点目标入组 70 人开始时间: 2021年7月9日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 70
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
- >= 20age old 至 ot applicable（—）
- 性别
- All
入选标准
- •1) Patients scheduled to undergo tracheal intubation for general anesthesia surgery
- •2) Patients with a preoperative ASA Physical Classification System (Class I or II).
- •Class I: No organic, physiological, biochemical, or psychological abnormalities. The disease to be operated on is localized and does not cause systemic (systematic) damage. The disease to be operated on is localized and does not cause systemic (systematic) damage.
- •Class II Mild to moderate systematic disorder. The causes are
- •The cause of the disorder is a disease that has been the subject of surgical treatment, or a condition other than the above, or a physiological cause. Physiological causes.
- •3) Patients who can give written consent to participate in this study and who are 20 years of age or older at the time of consent.
排除标准
- •1) Patients undergoing emergency surgery
- •2) Patients who need to be repositioned
- •3) Patients who are expected to have difficulty in intubation
研究者
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