Cross-sectional Study of Prevalence Rate of Abdominal Aortic Aneurysm in OSAHS Patients From BTCH
研究概览
地位
详细说明
Abdominal aortic aneurysm (AAA) is an extremely high mortality disease, and ultrasound has been recommended for the screening of AAA, which is highly sensitive and specific. Studies have shown that screening for AAA in the population can significantly reduce deaths from ruptured abdominal aortic aneurysms. However, those study mainly focus on cardiovascular disease patients or general population, no previous study target on obstructive sleep apnea hypopnea syndrome (OSAHS) population. Retrospective studies show that the incidence of apnea syndrome in patients with abdominal aortic aneurysm is higher than that in the control group, which suggests that OSAHS may be one of the causes of abdominal aortic aneurysm. At present, there is no relevant research on the screening of AAA in OSAHS population.
The main objective of this study was to screen the prevalence of AAA in OSAHS population by a cross-sectional study.
研究类型
注册 (预期的)
联系人和位置
学习地点
-
-
-
Beijing、中国、102218
- Beijing Tsinghua Changgung 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
取样方法
研究人群
描述
Inclusion Criteria:
- All patients who accept respiratory sleep monitoring in the department of ENT, BTCH, aged over 45 years, from 2018-01-01 to 2019-12-30
Exclusion Criteria:
- 1. Any previous diagnosis of AAA history;
- 2. Received AAA related treatment;
- 3. Past imaging test result suggested increased diameter of the abdominal aorta.
- 4. Poor compliance; refused to follow the requirements set in this study follow-up, and refused to sign informed consent.
学习计划
研究是如何设计的?
设计细节
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 |
|---|---|---|
|
Diameter of aorta
大体时间:0-48 hours
|
Diameter of aorta measured by ultrasound
|
0-48 hours
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
ABI
大体时间:0-48 hours
|
Ankel brachal index measured by Angiolab 2 - Phlebolab Doppler-System
|
0-48 hours
|
|
Carotid artery stenosis
大体时间:0-48 hours
|
Carotid artery stenosis measured by ultrasound
|
0-48 hours
|
合作者和调查者
调查人员
- 首席研究员:weiwei Wu, MD、Beijing Tsinghua Changgeng Hospital
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (预期的)
研究完成 (预期的)
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
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.