脊柱手术后对患者应用的三种不同方法对恶心，口渴和舒适的影响
The aim of this study was to determine the effects of postoperative methods on nausea, thirst and comfort levels of patients undergoing spinal surgery.
研究概览
详细说明
Within the scope of this randomized controlled study, it is aimed to evaluate the effectiveness of ice, mouthwash and menthol lozenge interventions to provide effects on postoperative nausea, thirst and comfort in patients undergoing spinal surgery
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
-
-
-
Amasya、土耳其（türkiye）
- Amasya Şerefeddin Sabuncuoğlu Hospital
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Adult patients who underwent lumbar disc herniation (LDH) surgery
- LDH surgery patients who recieve general anesthesia
- The patients who were conscious
- The duration of surgery is between 0-3 hours
Exclusion Criteria:
- Patients who cannot understand and speak Turkish
- Allergic patients to menthol
- Patients who received spinal anesthesia
- Patients with lesions on the oral mucosa and lips
- Patients requiring intensive care after surgical intervention
学习计划
研究是如何设计的？
设计细节
- 主要用途：支持治疗
- 分配：随机化
- 介入模型：并行分配
- 屏蔽：双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的：冰块
|
ıce cube |
|
实验性的：洗涤
|
Mouth wash |
|
实验性的：Menthol Lozenge
|
menthol lozenge |
|
无干预：Control group
Routine care |
研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Nausea
大体时间：once before the application and 60, 120, 180 and 240 min. after arrival at the clinic
|
Nausea level: It consists of a numeric scale. Among the numbers, ''0'' corresponds to ''no thirst/nausea'' and ''10'' corresponds to ''very much thirst/nausea''. As the number increases, nausea and thirst will be accepted as increased. There is no cut-off point. |
once before the application and 60, 120, 180 and 240 min. after arrival at the clinic
|
|
Thirst
大体时间：once before the application and 60, 120, 180 and 240 min. after arrival at the clinic
|
Thirst level: A minimum score of 12 and a maximum score of 60 can be obtained from the scale. The higher the score obtained from the scale, the higher the level of thirst discomfort of the patients. |
once before the application and 60, 120, 180 and 240 min. after arrival at the clinic
|
|
Comfort
大体时间：once before the application and 240 min. after arrival at the clinic
|
Comfort level: The highest score that can be obtained from the scale is 192 and the lowest score is 48. A high SCS scoring indicates a high comfort level of the individual. |
once before the application and 240 min. after arrival at the clinic
|
合作者和调查者
调查人员
- 首席研究员：Özge İşeri, PhD、Ondokuz Mayıs University
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
关键字
其他研究编号
- A.30.2.ODM.0.20.08/569-677
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)？
IPD 计划说明
Since this is a doctoral study, the results can be shared at the end of the thesis
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.