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- Ensaio Clínico NCT07834372
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.
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
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.
Tipo de estudo
Inscrição (Estimado)
Estágio
- Não aplicável
Contactos e Locais
Contato de estudo
- Nome: Whitney Huey
- Número de telefone: 877-478-3569
- E-mail: whuey@heartflow.com
Estude backup de contato
- Nome: Zachary Sterner, Ph.D
- Número de telefone: 877-478-3569
- E-mail: zsterner@heartflow.com
Locais de estudo
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North Carolina
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Greensboro, North Carolina, Estados Unidos, 27401
- REWRITE-CAD Trial Site
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Contato:
- Heartflow Investigator
- Número de telefone: 877-478-3569
- E-mail: rewrite-cad@heartflow.com
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
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)
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Prevenção
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Sem intervenção: Braço de Cuidados Habituais
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|
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Experimental: Unblinded AI-CPA Test Arm
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REWRITE-CAD will provide AI-CPA results |
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Prazo |
|---|---|
|
Percentage of participants who initiate or intensify lipid-lowering therapy (LLT)
Prazo: Enrollment to 90 days
|
Enrollment to 90 days
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Percentage of participants who initiate or intensify lipid-lowering therapy (LLT)
Prazo: 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
Prazo: Enrollment through end of study at 21 months
|
Enrollment through end of study at 21 months
|
|
|
Time to intensification of LLT
Prazo: Enrollment through end of study at 21 months
|
Enrollment through end of study at 21 months
|
|
|
% Undergoing lipid testing
Prazo: Enrollment through end of study at 21 months
|
Enrollment through end of study at 21 months
|
|
|
LDL-C changes
Prazo: Enrollment through end of study at 21 months
|
Enrollment through end of study at 21 months
|
|
|
Changes in Plaque Volumes
Prazo: Enrollment through end of study at 21 months
|
Enrollment through end of study at 21 months
|
|
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Referral to invasive coronary angiography (ICA) and coronary revascularization
Prazo: 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)
Prazo: 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
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- CP-912-001
Plano para dados de participantes individuais (IPD)
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