- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving 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.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
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.
Studietype
Registrering (Antatt)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiekontakt
- Navn: Whitney Huey
- Telefonnummer: 877-478-3569
- E-post: whuey@heartflow.com
Studer Kontakt Backup
- Navn: Zachary Sterner, Ph.D
- Telefonnummer: 877-478-3569
- E-post: zsterner@heartflow.com
Studiesteder
-
-
North Carolina
-
Greensboro, North Carolina, Forente stater, 27401
- REWRITE-CAD Trial Site
-
Ta kontakt med:
- Heartflow Investigator
- Telefonnummer: 877-478-3569
- E-post: rewrite-cad@heartflow.com
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
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
-
Symptoms suggestive of CAD (e.g. stable angina or dyspnea on exertion)
-
On PCSK9i and/or inclisiran at baseline
-
Reduced left ventricular ejection fraction (LVEF) <35%, if known
-
Prior coronary artery bypass graft (CABG)
-
Prior stents in 2+ vessel territories
-
Life expectancy less than 2 years due to non-CV comorbidities
-
Enrolled in an investigational trial that involves a non-approved cardiac drug or device
-
Previously evaluated with and/or in a trial which includes AI-CPA
-
Any condition that might interfere with trial procedures or follow up visits
-
LDL-C <70 mg/dL at baseline lab draw
-
Active chemotherapy and/or radiation
Imaging Based (all to be assessed by CCTA core lab)
-
Left Main (LM) ≥50% stenosis on baseline CCTA
-
Proximal LAD FFRct <0.75
-
Total occlusions in major vessels and/or total occlusion in stent
-
No visible plaque in non-stented segments on CCTA
-
Incidental findings requiring immediate follow-up or management (e.g., Aortic dissection, findings suggestive of cancer, pulmonary embolism)
-
Findings that require further imaging follow-up within 1 year (e.g., pulmonary nodules ≥6 mm)
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Forebygging
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Ingen inngripen: Vanlig omsorgsarm
|
|
|
Eksperimentell: Unblinded AI-CPA Test Arm
|
REWRITE-CAD will provide AI-CPA results |
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Percentage of participants who initiate or intensify lipid-lowering therapy (LLT)
Tidsramme: Enrollment to 90 days
|
Enrollment to 90 days
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Percentage of participants who initiate or intensify lipid-lowering therapy (LLT)
Tidsramme: 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
Tidsramme: Enrollment through end of study at 21 months
|
Enrollment through end of study at 21 months
|
|
|
Time to intensification of LLT
Tidsramme: Enrollment through end of study at 21 months
|
Enrollment through end of study at 21 months
|
|
|
% Undergoing lipid testing
Tidsramme: Enrollment through end of study at 21 months
|
Enrollment through end of study at 21 months
|
|
|
LDL-C changes
Tidsramme: Enrollment through end of study at 21 months
|
Enrollment through end of study at 21 months
|
|
|
Changes in Plaque Volumes
Tidsramme: 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
Tidsramme: 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)
Tidsramme: 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
|
Samarbeidspartnere og etterforskere
Sponsor
Samarbeidspartnere
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- CP-912-001
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
produkt produsert i og eksportert fra USA
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .