REWRITE-CAD Protocol: Risk Evaluation With AI-CPA to Reduce Progression and Improve Lifetime Care for Patients With Known Coronary Artery Disease (REWRITE-CAD)
Risk Evaluation With AI-CPA to Reduce Progression and Improve Lifetime Care for Patients With Known Coronary Artery Disease
REWRITE-CAD is a prospective, randomized, multi-center trial assessing the management of asymptomatic participants with a history of PCI or MI who will undergo a blinded CCTA and be randomly assigned to either the test arm in which participants receive the unblinded results of Heartflow AI-CPA or the usual care arm in which participants are blinded to the AI-CPA results.
研究概览
详细说明
The objective of the REWRITE-CAD trial is to assess changes in lipid lowering therapy over time in participants with a history of PCI or MI who undergo a blinded CCTA and are randomly assigned to either the test arm in which participants will undergo a blinded CCTA and receive the unblinded Heartflow AI-CPA results or the usual care arm in which participants will undergo a blinded CCTA with blinded AI-CPA results.
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Whitney Huey
- 电话号码:877-478-3569
- 邮箱:whuey@heartflow.com
研究联系人备份
- 姓名:Zachary Sterner, Ph.D
- 电话号码:877-478-3569
- 邮箱:zsterner@heartflow.com
学习地点
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North Carolina
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Greensboro、North Carolina、美国、27401
- REWRITE-CAD Trial Site
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接触:
- Heartflow Investigator
- 电话号码:877-478-3569
- 邮箱:rewrite-cad@heartflow.com
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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:
- History of PCI (1 year - 5 years prior to Day 0) and/or history of MI (Type I or II) (1 year - 5 years prior to Day 0)
- Patients who do not exhibit symptoms suggestive of CAD
- No other clinical CCTA subsequent to MI/PCI but prior to screening
- eGFR >45 mL/min per most recent measurement within 90 days
- Willingness to comply with all aspects of the protocol including research CCTAs, lab draws, medication adherence assessments, attending all study visits, and the ability to comply with prescribed medications
- For a female participant of childbearing potential (those who have not been surgically sterilized), a pregnancy test must be performed with negative results known within 7 days prior to randomization
- Ability to provide informed consent
- Visible plaque in non-stented region on CCTA as assessed by CCTA core lab
- Acceptable CCTA quality per Heartflow acceptance criteria
Exclusion Criteria:
Non-imaging based
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Symptoms suggestive of CAD (e.g. stable angina or dyspnea on exertion)
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On PCSK9i and/or inclisiran at baseline
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Reduced left ventricular ejection fraction (LVEF) <35%, if known
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Prior coronary artery bypass graft (CABG)
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Prior stents in 2+ vessel territories
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Life expectancy less than 2 years due to non-CV comorbidities
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Enrolled in an investigational trial that involves a non-approved cardiac drug or device
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Previously evaluated with and/or in a trial which includes AI-CPA
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Any condition that might interfere with trial procedures or follow up visits
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LDL-C <70 mg/dL at baseline lab draw
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Active chemotherapy and/or radiation
Imaging Based (all to be assessed by CCTA core lab)
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Left Main (LM) ≥50% stenosis on baseline CCTA
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Proximal LAD FFRct <0.75
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Total occlusions in major vessels and/or total occlusion in stent
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No visible plaque in non-stented segments on CCTA
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Incidental findings requiring immediate follow-up or management (e.g., Aortic dissection, findings suggestive of cancer, pulmonary embolism)
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Findings that require further imaging follow-up within 1 year (e.g., pulmonary nodules ≥6 mm)
学习计划
研究是如何设计的?
设计细节
- 主要用途:预防
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
无干预:日常护理臂
|
|
|
实验性的:Unblinded AI-CPA Test Arm
|
REWRITE-CAD will provide AI-CPA results |
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
Percentage of participants who initiate or intensify lipid-lowering therapy (LLT)
大体时间:Enrollment to 90 days
|
Enrollment to 90 days
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Percentage of participants who initiate or intensify lipid-lowering therapy (LLT)
大体时间:Enrollment through end of study at 21 months
|
Enrollment through end of study at 21 months
|
|
|
Percentage of participants who initiate or intensify cardiovascular disease prevention medication therapy
大体时间:Enrollment through end of study at 21 months
|
Enrollment through end of study at 21 months
|
|
|
Time to intensification of LLT
大体时间:Enrollment through end of study at 21 months
|
Enrollment through end of study at 21 months
|
|
|
% Undergoing lipid testing
大体时间:Enrollment through end of study at 21 months
|
Enrollment through end of study at 21 months
|
|
|
LDL-C changes
大体时间:Enrollment through end of study at 21 months
|
Enrollment through end of study at 21 months
|
|
|
Changes in Plaque Volumes
大体时间:Enrollment through end of study at 21 months
|
Enrollment through end of study at 21 months
|
|
|
Referral to invasive coronary angiography (ICA) and coronary revascularization
大体时间:Enrollment through end of study at 21 months
|
Enrollment through end of study at 21 months
|
|
|
Percentage of participants classified as high adherence on the 8-item Morisky Medication Adherence Scale (MMAS-8)
大体时间:Enrollment through end of study at 21 months
|
Evaluated using the 8-item MMAS-8 questionnaire. Total scores range from 0 to 8, where higher scores indicate better adherence. High adherence is defined as achieving a score of 8, medium adherence as 6 to <8, and low adherence as <6. |
Enrollment through end of study at 21 months
|
合作者和调查者
合作者
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
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
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