Artificial Intelligence (AI) for Proximal Caries Detection and Its Impact on Treatment Threshold
2026年8月27日 更新者:Margherita Fontana、University of Michigan
Artificial Intelligence for Proximal Caries Detection and Its Impact on Treatment Threshold: Randomized Trial
The purpose of this study is to assess the impact of artificial intelligence on proximal caries detection and subsequent treatment decisions of early learners and compare those with outcomes of experienced learners.
研究概览
研究类型
介入性
注册 (估计的)
60
阶段
- 不适用
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。
学习联系方式
- 姓名:Carmen Boren, DDS, FAGD
- 电话号码:701-240-8191
- 邮箱:drcarmen@umich.edu
学习地点
-
-
Michigan
-
Ann Arbor、Michigan、美国、48109
- 招聘中
- University of Michigan
-
接触:
- Carmen Boren
- 邮箱:drcarmen@umich.edu
-
首席研究员:
- Margherita Fontana, DDS, PhD
-
-
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
- 成人
- 年长者
接受健康志愿者
不
描述
Early learner Inclusion Criteria:
- Provide informed consent
- Willing to comply with all study procedures and be available for the duration of the study
- Dental student in second, third, or fourth year of dental school at University of Michigan School of Dentistry
Late learner Inclusion Criteria:
- Provide informed consent
- Willing to comply with all study procedures and be available for the duration of the study
- Dental resident or junior faculty having at least 2 years of clinical experience outside of a dental education setting
Exclusion Criteria for participants:
- Dental students who do not have previous experience with caries detection (such as first year dental students)
- Residents that do not have frequent exposure to caries detection, such as orthodontic, periodontic, oral surgery graduate residents.
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
- 主要用途:其他
- 分配:随机化
- 介入模型:交叉作业
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
其他:Early Learners - Dental students
|
Participants will be asked to attend two visits and view a randomized series of dental radiographs (10 at each visit).
Participants will answer a set of questions for each image reviewed.
Some of the radiographs will have an Artificial Intelligence enhancement and some will not.
Participants will be asked to return within about one week of the first visit to view the second set of x-rays and answer the survey questions.
|
|
其他:Late Learners - Dental resident or junior faculty
|
Participants will be asked to attend two visits and view a randomized series of dental radiographs (10 at each visit).
Participants will answer a set of questions for each image reviewed.
Some of the radiographs will have an Artificial Intelligence enhancement and some will not.
Participants will be asked to return within about one week of the first visit to view the second set of x-rays and answer the survey questions.
|
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 |
|---|---|---|
|
Lesion severity
大体时间:approximately 1 week (2 sessions)
|
Levels for this outcome will be sound, outer enamel, inner enamel/outer dentin, inner dentin.
|
approximately 1 week (2 sessions)
|
|
Diagnostic accuracy
大体时间:Approximately 1 week (2 sessions)
|
Approximately 1 week (2 sessions)
|
|
|
Specificity
大体时间:Approximately 1 week (2 sessions)
|
Approximately 1 week (2 sessions)
|
|
|
Overall sensitivity
大体时间:Approximately 1 week (2 sessions)
|
Approximately 1 week (2 sessions)
|
|
|
Sensitivity for outer enamel
大体时间:Approximately 1 week (2 sessions)
|
Approximately 1 week (2 sessions)
|
|
|
Sensitivity for inner enamel/outer dentin
大体时间:Approximately 1 week (2 sessions)
|
Approximately 1 week (2 sessions)
|
|
|
Sensitivity for inner dentin
大体时间:Approximately 1 week (2 sessions)
|
Approximately 1 week (2 sessions)
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Intervention
大体时间:approximately 1 week (2 sessions)
|
(levels for this outcome will be none, non-restorative, restorative)
|
approximately 1 week (2 sessions)
|
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:Margherita Fontana, DDS, PhD、University of Michigan
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 (估计的)
2026年9月1日
初级完成 (估计的)
2027年5月1日
研究完成 (估计的)
2027年5月1日
研究注册日期
首次提交
2026年6月9日
首先提交符合 QC 标准的
2026年6月9日
首次发布 (实际的)
2026年6月15日
研究记录更新
最后更新发布 (实际的)
2026年8月28日
上次提交的符合 QC 标准的更新
2026年8月27日
最后验证
2026年8月1日
更多信息
与本研究相关的术语
其他研究编号
- HUM00276058
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
不
IPD 计划说明
Interested parties and contact the PI for potential collaboration
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
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.