The Impact of Comprehensive Education Before Gastroscopy on Improving the Tolerance of Patients
The Impact of Comprehensive Education Before Gastroscopy on Improving the Tolerance of Patients: A Prospective Randomized Controlled Study
研究概览
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
-
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Zhejiang
-
Ningbo、Zhejiang、中国、315010
- Ningbo NO.1 hospital
-
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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:
- Patients over the age of 18 years undergoing routine gastroscopy
- Informed consent
Exclusion Criteria:
- Serious coronary heart disease and myocardial injury with serious heart failure
- Stenosis of the esophagus or cardia obstruction
- Acute pharyngitis and tonsillitis
- Acute upper gastrointestinal bleeding
- Hemodynamically unstable
- allergy to topical lidocaine
- Patients did not cooperate or spirit was not normal
- Pregnancy
学习计划
研究是如何设计的?
设计细节
- 主要用途:诊断
- 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:Comprehensive education group
The details of Comprehensive education are as follows:
|
The details of Comprehensive education are as follows:
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|
无干预:standard education
The details of standard education are as follows:
|
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 |
|---|---|---|
|
Adverse reaction times in gastroscopy
大体时间:1 day
|
research assistant records nausea/vomiting/retching times in the whole process of gastroscopy
|
1 day
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Patients' tolerance scores
大体时间:1 day
|
At the end of the procedure, the patients were asked about the tolerance in the process of gastroscopy by using a 100-mm visual analogue scale.
Tolerance includes the extent of pain and nausea.
The endpoints were assigned "no nausea or no pain " to the left and "worst possible nausea or worst pain imaginable " to the right.
|
1 day
|
其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Endoscopists' assessment scores
大体时间:1 day
|
At the end of the procedure, Endoscopists scored the level of difficulty in introduction of the gastroscope on a 100-mm visual analogue scale. The endpoints were assigned " easiest" to the left and " worst difficult " to the right. Endoscopists' satisfaction was assessed with 100-mm VAS for the performances of the endoscopes. The endpoints were assigned " worst dissatisfied" to the left and " Most satisfied " to the right. |
1 day
|
|
Systolic/diastolic blood pressure (SBP/DBP)
大体时间:1 day
|
Patients were monitored the Systolic/diastolic blood pressure (SBP/DBP) throughout using an electronic multifunctional patient monitor unit.
The research assistant records Systolic/diastolic blood pressure (SBP/DBP) on 5 min prior to endoscopic intubation, during endoscopy and at time of entry into the stomach body
|
1 day
|
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Pulse rate (PR)
大体时间:1 day
|
Patients were monitored the pulse rate (PR) throughout using an electronic multifunctional patient monitor unit.
The research assistant records pulse rate (PR) on 5 min prior to endoscopic intubation, during endoscopy and at time of entry into the stomach body.
|
1 day
|
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Oxygen saturation by pulse oximetry (SpO2)
大体时间:1 day
|
Patients were monitored the Oxygen saturation by pulse oximetry (SpO2) throughout using an electronic multifunctional patient monitor unit.
The research assistant records oxygen saturation by pulse oximetry (SpO2) on 5 min prior to endoscopic intubation, during endoscopy and at time of entry into the stomach body.
|
1 day
|
合作者和调查者
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
其他研究编号
- 2018-R010
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
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
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