jRCTs072240066招募中不适用
Non-randomized trial to evaluate the efficacy and safety of the Nociception Level Index in supine surgery patients (NOL study)
未提供0 个研究点目标入组 110 人开始时间: 待定最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 110
- 主要终点
- -
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomized Controlled Trial
- 干预模型
- Parallel Assignment
- 主要目的
- Other
- 盲法
- Open(masking Not Used)
入排标准
- 年龄范围
- 16age old over 至 79age old under（—）
- 性别
- All
入选标准
- •Participants undergoing posterior spinal fusion surgery (open surgery)
- •Participants who have given their own voluntary written consent (for retrospective study participants, those who can opt out of the study)
- •Participants aged 16 to 79 years at the time of consent
- •Participants weighing 30kg or more
- •Participants with ASA-PS of I to III before the start of the study
排除标准
- •Participants with arrhythmia
- •Participants with a history of drug hypersensitivity (propofol, remifentanil, and/or fentanyl)
- •Participants taking steroids
- •Endoscopic surgery, anterior cervical discectomy and fusion
- •Participants who the principal investigator judges inappropriate for inclusion in the study
结局指标
主要结局
-
Intraoperative remifentanil dose
次要结局
- Vasoactive medication
- Hypotension
- Hypertension
- Bradycardia
- Tachycardia
- Stress hormone levels
- Total dose of postoperative analgesics(24 hours)
- Serum creatinine and troponin levels
研究者
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