NCT05106452Unknown不适用
Intraoperative Analgesia Management in Gynecological Surgery With Erector Spinae Block
Zonguldak Bulent Ecevit University1 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2021年10月20日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 35
- 试验地点
- 1
- 主要终点
- intraoperative opioid consumption
研究概览
简要总结
The aim of the study is to compare the analgesic nociception index (ANI), which is used to determine the dose of analgesic agent needed in the intraoperative period, with the conventional method in patients with erector spinae block who underwent gynecological surgery under general anesthesia.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •ASA I-II-III risk group
- •Patients who underwent gynecological surgery under general anesthesia, who underwent erector spina block, and whose pain was followed by analgesia nociception index or conventional methods for intraoperative pain monitoring
- •Patients whose informed consent was read and consent was obtained from them and their guardians
排除标准
- •cardiac rhythm disorder
- •central-autonomic nervous system disease
- •neuropsychiatric disease
- •receiving opioid therapy
- •Use of drugs that will affect cardiac autonomic regulation
- •Known allergy to the drugs to be applied
- •Contraindicated for ESP block
- •Patients who do not agree to participate in the study will not be included in the study.
- •Patients who were administered drugs to stabilize the patient's hemodynamics during the operation
结局指标
主要结局
intraoperative opioid consumption
时间窗: during the surgery
Effect of ANI monitoring on intraoperative opioid consumption
次要结局
- nausea and vomiting i(during her stay in the recovery unit)
- VAS pain scores(during her stay in the recovery unit)
- duration of stay in recovery room(at the end of the surgery)
- emergence time(at the end of the surgery)
研究者
Çağdaş Baytar
assistant professor
Zonguldak Bulent Ecevit University
研究点 (1)
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