OSUWMC EEI Sequential Cataract Patient Experience Project
2018年4月10日 更新者：Deborah Lowery、Ohio State University
The purpose is to gauge the patients' level of comfort and anxiety for sequential cataract surgeries to assess if the second experience of cataract surgery differs from the initial experience.
研究概览
详细说明
Each patient is scheduled to undergo two sequential cataract extractions under topical anesthesia with local anesthetic eye drops and minimal sedation- one on each eye.
The surgeon, basic surgical procedure, anesthetic technique, and approximate length of procedure are reasonably similar and the patients act as their own control.
Subjects in the study will answer very brief questions regarding anxiety and comfort about their surgery before and after each procedure, and on the day after their second surgery.
研究类型
观察性的
注册 (实际的)
286
联系人和位置
本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。
学习地点
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Ohio
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Columbus、Ohio、美国、43210
- The Ohio State University Wexner Medical Center
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参与标准
研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 及以上 (成人、年长者)
接受健康志愿者
是的
有资格学习的性别
全部
取样方法
非概率样本
研究人群
Patients will be identified by their status presenting for surgery with one specific surgeon (A.T.) at the Eye and Ear Center at Gowdy Fields.
Access will be through the preoperative anesthesia assessment performed by the attending anesthesiologist.
描述
Inclusion Criteria:
- Patients undergoing sequential cataract surgeries within a 6 week time period performed by the ophthalmologist, Amit Tandon, MD.
- Aged 18 years and older.
Exclusion Criteria:
- Cognitive impairment causing inability to participate in survey
- Language barrier causing an inability to participate in survey
- Healthcare POA or guardian leading to an inability to consent to survey
- Physician autonomy; patients that are inappropriate for the study as deemed by investigator
学习计划
本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。
研究是如何设计的？
设计细节
队列和干预
团体/队列 |
干预/治疗 |
|---|---|
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Sequential Cataract Surgery with Survey
Subjects eligible for the study will fall into the sequential cataract surgery group and be administered brief surveys.
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Verbal survey will be given before and after the cataract surgery, and on the day following the second cataract surgery.
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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 |
|---|---|---|
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Pain
大体时间：First and second cataract extraction surgery occuring within 6 weeks
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Pain will be evaluated using verbal survey after each cataract surgery, scheduled to occur within 6 weeks time; subject will be asked if there was any difference in pain between surgeries on the day after the second cataract surgery.
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First and second cataract extraction surgery occuring within 6 weeks
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Anxiety
大体时间：First and second cataract extraction surgery occuring within 6 weeks
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Anxiety will be evaluated using verbal survey before each cataract surgeries, scheduled to occur within 6 weeks time; subject will be asked if there was any difference in anxiety between surgeries on the day after the second cataract surgery.
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First and second cataract extraction surgery occuring within 6 weeks
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Awareness
大体时间：First and second cataract extraction surgery occuring within 6 weeks
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Awareness will be evaluated using verbal survey after each cataract surgeries, scheduled to occur within 6 weeks time; subject will be asked if there was any difference in awareness between surgeries on the day after the second cataract surgery.
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First and second cataract extraction surgery occuring within 6 weeks
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Comfort Level
大体时间：First and second cataract extraction surgery occuring within 6 weeks
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Comfort level will be evaluated using verbal survey after cataract surgeries, scheduled to occur within 6 weeks time; subject will be asked if there was any difference in comfort level between surgeries on the day after the second cataract surgery.
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First and second cataract extraction surgery occuring within 6 weeks
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员：Deborah Lowery, MD、Ohio State University
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2017年1月1日
初级完成 (实际的)
2018年3月1日
研究完成 (实际的)
2018年3月1日
研究注册日期
首次提交
2016年12月15日
首先提交符合 QC 标准的
2016年12月21日
首次发布 (估计)
2016年12月26日
研究记录更新
最后更新发布 (实际的)
2018年4月11日
上次提交的符合 QC 标准的更新
2018年4月10日
最后验证
2018年4月1日
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.
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