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Optical Coherence Tomography of the Saphenous Vein Graft (OCTOCAB)

4. Mai 2022 aktualisiert von: Ziad Ali, MD, DPhil, St. Francis Hospital, New York

Intraoperative Optical Coherence Tomography of the Saphenous Vein Conduit in Patients Undergoing Coronary Artery Bypass Surgery

OCTOCAB is a prospective, randomized (1:1), single-center trial. The purpose of this study is to determine whether intravascular optical coherence tomography (OCT) guided saphenous vein grafting in coronary artery bypass surgery will reduce the rate of early vein graft failure (VGF).

Studienübersicht

Status

Rekrutierung

Detaillierte Beschreibung

Within the first year of coronary artery bypass grafting (CABG) surgery, the saphenous vein grafts have a failure rate of 10 to 25%. Visual inspection of the vein graft conduit is the current standard in determining the quality of the vein segment. However, there may be intraluminal abnormalities that are undetectable via a visual inspection. OCT examination, using the ILUMIEN OPTIS NEXT OCT Imaging system, of endoscopically harvested saphenous vein conduits will indicate such pathology and enable the surgeon to assess the quality of the harvested vein at the intravascular level.

This study is designed to demonstrate the superiority of OCT-guided saphenous vein CABG in improving the rates of early VGF and the overall outcome of CABG.

The study will follow two randomization arms: OCT-guided saphenous vein CABG (interventional arm) vs. visual inspection-guided saphenous vein CABG (standard of care arm). The analysis of subjects will be with respect to their analyzed group.

Following enrollment, participants will be followed for up to 10 years. The primary endpoint is per graft incidence of vein graft failure. The assessment of the vein graft will be conducted via coronary CT angiogram (CCTA) at 12 months. In the case where the participant has unplanned angiogram due to clinical reasons, prior to the 12 months, the condition of the graft will be determined via the angiogram. Unless all target grafts have reached the endpoint prior to the 12 month time point, a CCTA will be required.

To achieve the power level of 85% at the significance level of 0.025, 760 patients is the anticipated sample size. Analysis will be conducted at the graft level with a Linear Mixed model to account for any potential patient effects.

Studientyp

Interventionell

Einschreibung (Voraussichtlich)

760

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studieren Sie die Kontaktsicherung

Studienorte

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre und älter (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  1. Subject must be at least 18 years of age.
  2. Subject must have evidence of myocardial ischemia (e.g., stable angina, silent ischemia (ischemia in the absence of chest pain or other anginal equivalents), unstable angina, or acute myocardial infarction) suitable for elective CABG.
  3. Subject must have undergone coronary angiography identifying at least one lesion that is clinically appropriate and suitable for saphenous vein bypass grafting.
  4. Subject must provide written Informed Consent prior to any study related procedure.

Exclusion Criteria:

  1. STEMI ≤24 hours from the onset of ischemic symptoms
  2. Creatinine clearance ≤30 ml/min/1.73 m2 (as calculated by MDRD formula for estimated GFR) and not on dialysis.
  3. Hypotension, shock or need for mechanical support or intravenous vasopressors at the time that the patient would be undergoing the index procedure.
  4. CHF (Killip class >2 or NYHA class >3)
  5. LVEF <30% by the most recent imaging test within 6 months prior to procedure. If no LVEF test result within 6 months is available, it must be assessed by echocardiography, multiple gated acquisition (MUGA), magnetic resonance imaging (MRI), ventriculography (LV gram) or other method.
  6. Unstable ventricular arrhythmias
  7. Concomitant multi-valve surgery or major aortic root surgery.
  8. Planned non-cardiac surgery within 24 months after the index procedure
  9. Prior CABG
  10. Any planned PCI within any target vessel(s) within 24 months.
  11. Subject has known hypersensitivity or contraindication to any of the study drugs (including aspirin, all P2Y12 inhibitors).
  12. Subject has received a heart transplant.
  13. Subject is receiving immunosuppressant therapy or has known immunosuppressive or severe autoimmune disease that requires chronic immunosuppressive therapy (e.g., human immunodeficiency virus, systemic lupus erythematosus, etc.).
  14. Subject has previously received or is scheduled to receive radiotherapy to a coronary artery (vascular brachytherapy), or the chest/mediastinum.
  15. Subject has a platelet count <100,000 cells/mm3 or >700,000 cells/mm3.
  16. Subject has a documented or suspected hepatic disorder as defined as cirrhosis or Child-Pugh ≥ Class B.
  17. Subject has a history of bleeding diathesis or coagulopathy.
  18. Subject has life expectancy <2 years for any non-cardiac cause.
  19. Pregnant or nursing subjects and those who plan pregnancy in the period up to 2 years following index procedure. Female subjects of child-bearing potential must have a negative pregnancy test done within 7 days prior to the index procedure per site standard test.
  20. Presence of other anatomic or comorbid conditions, or other medical, social, or psychological conditions that, in the investigator's opinion, could limit the subject's ability to participate in the clinical investigation or to comply with follow-up requirements, or impact the scientific soundness of the clinical investigation results.

Conduit exclusion criteria

1. Severe conduit tortuosity of venous conduit (e.g., with varicosities) such that it is unlikely that the OCT catheter can be delivered without vascular damage.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Verdreifachen

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: OCT-guided saphenous vein graft coronary artery bypass graft surgery
Optical Coherence Tomography (OCT) provides high quality intravascular images by using infrared light. OCT will assess the harvested saphenous vein conduit in Coronary Bypass Graft Surgery (CABG). Abnormalities found in the harvested conduits via OCT, at the discretion of the surgeon, will not be utilized for CABG.
OCT examination of harvested saphenous vein conduits will indicate pathology. Under the surgeon's discretion the conduit segments with pathology will not be grafted.
Andere Namen:
  • ILUMIEN OPTIS NEXT OCT Imaging System
  • ILUMIEN OPTIS OCT Imaging System
  • OPTIS Integrated OCT Imaging System
  • OPTIS Mobile OCT Imaging System
  • Dragonfly Duo Catheter
  • Dragonfly OPTIS Catheter
  • Dragonfly OpStar Imaging Catheter
  • Dual Channel AureFlo Systems
  • Coronary Flowprobes
Kein Eingriff: Visual inspection-guided saphenous vein graft coronary artery graft surgery
Harvested saphenous vein conduits will be assessed visually and will undergo a blinded OCT.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Vein graft failure (VGF)
Zeitfenster: 12 months
Per graft incidence of VGF defined as greater than or equal to 70% in the body of the graft on coronary CT angiography (CCTA)
12 months

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Gesamtmortalität
Zeitfenster: 12 Monate
12 Monate
Target graft failure (TGF)
Zeitfenster: 12 months
Composite time-to-first event rate of cardiac death, target graft myocardial infarction (TG-MI), or ischemia-driven target graft revascularization (ID-TGR)
12 months
Per graft incidence of ischemic vein graft failure
Zeitfenster: 12 months
Greater than or equal to 70% stenosis
12 months
Per graft incidence anatomic vein graft failure
Zeitfenster: 12 months
Greater than or equal to 50% stenosis
12 months
Per patient incidence of vein graft patency
Zeitfenster: 12 months
Vein graft having less than 50% stenosis
12 months
Per patient incidence of ischemic vein graft failure
Zeitfenster: 12 months
Greater than or equal to 70% stenosis
12 months
Per patient incidence of anatomic vein graft failure
Zeitfenster: 12 months
Greater than or equal to 50% stenosis
12 months
Mean vein graft diameter stenosis
Zeitfenster: 12 months
12 months
Mean vein graft area stenosis
Zeitfenster: 12 months
12 months
Cardiac and non-cardiac mortality
Zeitfenster: 12 months
12 months
All Myocardial Infarction (MI)
Zeitfenster: 12 months
12 months
Target graft myocardial infarction (TG-MI) and Non-Target graft myocardial infarction (non-TG-MI)
Zeitfenster: 12 months
12 months
All revascularization
Zeitfenster: 12 months
12 months
Ischemia driven (ID)-revascularization and Non-ischemia driven (ID)-revascularization
Zeitfenster: 12 months
12 months
Ischemia driven-target graft failure (ID-TGR)
Zeitfenster: 12 months
12 months
Ischemia driven (ID)-revascularization of target native coronary artery subtended by the graft
Zeitfenster: 12 months
12 months

Andere Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Intimal injury
Zeitfenster: 12 months
Major - Disruption of intima with arc ≥ 60˚ AND length: ≥ 2 mm Minor - Disruption of intima with arc <60˚ AND length: <2 mm
12 months
Intraluminal mass
Zeitfenster: 12 months
Major - Mass extending ≥ 5 cm and ≥ 2 mm in diameter Minor - Mass extending < 5 cm and < 2 mm in diameter
12 months
Intramural hematoma
Zeitfenster: 12 months
Major - ≥ 60˚ arc and length ≥ 5mm Minor - < 60˚ arc and length < 5mm
12 months
Valvular sclerosis
Zeitfenster: 12 months
Major - > 0.25mm thickness Minor - ≤ 0.25mm thickness with redundant valve tissue
12 months
Immunohistochemistry
Zeitfenster: 12 months
Relationship between the OCT-identified abnormalities with immunohistochemistry in the surplus and OCT-guided excluded segments of vein grafts for histological validation of OCT-identified abnormal findings.
12 months
Transit-Time Flow Meter (TTFM)
Zeitfenster: 12 months
All grafts will be assessed with TTFM to assess anastomosis. Data will be reviewed to determine whether TTFM abnormalities correlated to OCT findings.
12 months
Relationship between OCT parameters and endpoint rates
Zeitfenster: 12 months
12 months
Relationship between OCT parameters at baseline in the standard of care arm with OCT findings in vivo during follow-up
Zeitfenster: 12 months
12 months

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Hauptermittler: Ziad A. Ali, MD,DPhil, Saint Francis Memorial Hospital
  • Hauptermittler: Edward F. Lundy, MD, PhD, Saint Francis Memorial Hospital

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Allgemeine Veröffentlichungen

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

4. April 2022

Primärer Abschluss (Voraussichtlich)

4. April 2024

Studienabschluss (Voraussichtlich)

4. April 2026

Studienanmeldedaten

Zuerst eingereicht

15. November 2021

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

15. November 2021

Zuerst gepostet (Tatsächlich)

22. November 2021

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

5. Mai 2022

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

4. Mai 2022

Zuletzt verifiziert

1. Mai 2022

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Ja

Produkt, das in den USA hergestellt und aus den USA exportiert wird

Ja

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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